| Approved symbol | NKX2-1 |
|---|---|
| Approved name | NK2 homeobox 1 |
| HGCN ID | HGNC:11825 |
| Previous symbols | NKX2A, BCH, TITF1 |
| Inheritance | |
| OMIM | 600635 |
| Chromosome | 14q13.3 |
| Panel(s) |
NGS Hypothyroidism NGS Intellectual disability NGS Interstitial lung disease ILD NGS Mendeliome NGS Movement disorders NKX2-1 Analysis |
