| Approved symbol | ATP6V0A2 |
|---|---|
| Approved name | ATPase H+ transporting V0 subunit a2 |
| HGCN ID | HGNC:18481 |
| Previous symbols | |
| Inheritance | |
| OMIM | 611716 |
| Chromosome | 12q24.31 |
| Panel(s) |
NGS Cutis laxa and related disorders NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Skeletal Dysplasia NGS Treatable metabolic neurodegenerative disorders |
