| Approved symbol | AMT |
|---|---|
| Approved name | aminomethyltransferase |
| HGCN ID | HGNC:473 |
| Previous symbols | |
| Inheritance | |
| OMIM | 238310 |
| Chromosome | 3p21.31 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders NGS White matter disease |
