| Approved symbol | IFT52 |
|---|---|
| Approved name | intraflagellar transport 52 |
| HGCN ID | HGNC:15901 |
| Previous symbols | C20orf9 |
| Inheritance | |
| OMIM | 617094 |
| Chromosome | 20q13.12 |
| Panel(s) |
NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Skeletal Dysplasia |
