| Approved symbol | CAPN5 |
|---|---|
| Approved name | calpain 5 |
| HGCN ID | HGNC:1482 |
| Previous symbols | VRNI |
| Inheritance | |
| OMIM | 602537 |
| Chromosome | 11q13.5 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
