| Approved symbol | SLC19A3 |
|---|---|
| Approved name | solute carrier family 19 member 3 |
| HGCN ID | HGNC:16266 |
| Previous symbols | |
| Inheritance | |
| OMIM | 606152 |
| Chromosome | 2q36.3 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS White matter disease |
