| 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 Bewegingsstoornissen NGS Epilepsie NGS Intellectual disability NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Wittestofziekten |
