| Approved symbol | UNC13A |
|---|---|
| Approved name | unc-13 homolog A |
| HGCN ID | HGNC:23150 |
| Previous symbols | |
| Inheritance | |
| OMIM | 609894 |
| Chromosome | 19p13.11 |
| Panel(s) |
NGS Amyotrophic lateral sclerosis ALS NGS Intellectual disability NGS Mendeliome NGS Muscle disorders |
