| Approved symbol | AMPD2 |
|---|---|
| Approved name | adenosine monophosphate deaminase 2 |
| HGCN ID | HGNC:469 |
| Previous symbols | |
| Inheritance | |
| OMIM | 102771 |
| Chromosome | 1p13.3 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Microcephaly NGS Movement disorders NGS Pontocerebellar hypoplasia PCH NGS Preconception panel (for consanguineous couples) |
