| Approved symbol | CC2D2A |
|---|---|
| Approved name | coiled-coil and C2 domain containing 2A |
| HGCN ID | HGNC:29253 |
| Previous symbols | |
| Inheritance | |
| OMIM | 612013 |
| Chromosome | 4p15.32 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Skeletal Dysplasia NGS Vision disorder CSNB |
