81190 Cstb gene known famil vrnt
Pathology & Lab
Also known as: CSTB familial variant testing, CSTB targeted analysis
Targeted mutation analysis of the CSTB gene to identify known familial variants associated with Progressive Myoclonic Epilepsy type 1.
Clinical Context
Used to identify known CSTB pathogenic variants in family members of affected individuals for genetic counseling and disease prediction.
RVU Breakdown
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| Practice Expense RVU | 0.00 |
| Malpractice RVU | 0.00 |
| Total RVU | 0.00 |
Specialties
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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.