| Approved symbol | IFT27 |
|---|---|
| Approved name | intraflagellar transport 27 |
| HGCN ID | HGNC:18626 |
| Previous symbols | RABL4 |
| Inheritance | |
| OMIM | 615870 |
| Chromosome | 22q12.3 |
| 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 |
