| Approved symbol | CACNA2D4 |
|---|---|
| Approved name | calcium voltage-gated channel auxiliary subunit alpha2delta 4 |
| HGCN ID | HGNC:20202 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608171 |
| Chromosome | 12p13.33 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Congenital stationary nightblindness NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
