81338 Mpl gene common variants
Also known as: MPL mutation test, myeloproliferative neoplasm screening
Myeloproliferative Leukemia Virus Oncogene (MPL) gene analysis for common variants in myeloproliferative neoplasms.
In Plain Language
Blood cancer mutation test; Platelet disorder genetic test
Clinical Context
Detects MPL mutations in myeloproliferative neoplasms, particularly essential thrombocythemia and primary myelofibrosis.
RVU Information
CPT 81338 does not have a physician work RVU assigned by CMS. Reimbursement for this code is determined by payer-specific fee schedules.
Billing & Documentation
Lab and pathology codes require an order from the treating provider with clinical indication. For molecular pathology and genetic testing, document the specific analytes tested and clinical rationale.
How This Code Compares
This code has a work RVU of 0.00, meaning it does not have a physician work component assigned by CMS. In the Pathology & Lab category, 94% of codes share this characteristic.
Specialties
Frequently Asked Questions
What is CPT code 81338?
CPT 81338 (Mpl gene common variants) is a Pathology & Lab code. Myeloproliferative Leukemia Virus Oncogene (MPL) gene analysis for common variants in myeloproliferative neoplasms.
Who uses CPT code 81338?
CPT 81338 is used by Pathology, Hematology, Oncology. Detects MPL mutations in myeloproliferative neoplasms, particularly essential thrombocythemia and primary myelofibrosis.
When is CPT 81338 used?
Detects MPL mutations in myeloproliferative neoplasms, particularly essential thrombocythemia and primary myelofibrosis.
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CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.