| Approved symbol | NKX6-2 |
|---|---|
| Approved name | NK6 homeobox 2 |
| HGCN ID | HGNC:19321 |
| Previous symbols | |
| Inheritance | |
| OMIM | 605955 |
| Chromosome | 10q26.3 |
| Panel(s) |
NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS White matter disease |
