| Approved symbol | KCNV2 |
|---|---|
| Approved name | potassium voltage-gated channel modifier subfamily V member 2 |
| HGCN ID | HGNC:19698 |
| Previous symbols | |
| Inheritance | |
| OMIM | 607604 |
| Chromosome | 9p24.2 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
