81302 Mecp2 gene full seq
Also known as: MECP2 full sequencing, Rett syndrome genetic test
Methyl-CpG-binding protein 2 (MECP2) gene full gene sequence analysis to identify variants causing Rett syndrome.
In Plain Language
Brain developmental disorder genetic test; Rett syndrome screening
Clinical Context
Full MECP2 sequencing for Rett syndrome diagnosis in females presenting with developmental regression and autistic features.
RVU Information
CPT 81302 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 81302?
CPT 81302 (Mecp2 gene full seq) is a Pathology & Lab code. Methyl-CpG-binding protein 2 (MECP2) gene full gene sequence analysis to identify variants causing Rett syndrome.
Who uses CPT code 81302?
CPT 81302 is used by Pathology, Neurology, Genetics. Full MECP2 sequencing for Rett syndrome diagnosis in females presenting with developmental regression and autistic features.
When is CPT 81302 used?
Full MECP2 sequencing for Rett syndrome diagnosis in females presenting with developmental regression and autistic features.
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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.