81189 Cstb gene full gene sequence
Pathology & Lab
Also known as: CSTB sequencing, CSTB full analysis
Complete sequence analysis of the CSTB gene to identify point mutations and small indels associated with Progressive Myoclonic Epilepsy type 1.
Clinical Context
Employed to comprehensively screen for CSTB mutations in patients with progressive myoclonic epilepsy for diagnostic confirmation.
RVU Breakdown
| Work RVU | 0.00 |
| Practice Expense RVU | 0.00 |
| Malpractice RVU | 0.00 |
| Total RVU | 0.00 |
Specialties
Track This Code in RVU Edge
Log procedures, calculate wRVUs, and benchmark against MGMA data — all in one app.
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.