| Approved symbol | COX6B1 |
|---|---|
| Approved name | cytochrome c oxidase subunit 6B1 |
| HGCN ID | HGNC:2280 |
| Previous symbols | COX6B |
| Inheritance | |
| OMIM | 124089 |
| Chromosome | 19q13.12 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS White matter disease |
