| Approved symbol | EIF2B1 |
|---|---|
| Approved name | eukaryotic translation initiation factor 2B subunit alpha |
| HGCN ID | HGNC:3257 |
| Previous symbols | EIF2B |
| Inheritance | |
| OMIM | 606686 |
| Chromosome | 12q24.31 |
| Panel(s) |
NGS Dementia/ALS NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS White matter disease |
