| Approved symbol | TUBA1A |
|---|---|
| Approved name | tubulin alpha 1a |
| HGCN ID | HGNC:20766 |
| Previous symbols | |
| Inheritance | |
| OMIM | 602529 |
| Chromosome | 12q13.12 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Microcephaly NGS Movement disorders NGS Pontocerebellar hypoplasia PCH |
