| Approved symbol | IFT74 |
|---|---|
| Approved name | intraflagellar transport 74 |
| HGCN ID | HGNC:21424 |
| Previous symbols | CCDC2 |
| Inheritance | |
| OMIM | 608040 |
| Chromosome | 9p21.2 |
| 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 |
