| Approved symbol | SLC16A2 |
|---|---|
| Approved name | solute carrier family 16 member 2 |
| HGCN ID | HGNC:10923 |
| Previous symbols | DXS128, AHDS, MRX22 |
| Inheritance | |
| OMIM | 300095 |
| Chromosome | Xq13.2 |
| Panel(s) |
NGS Bewegingsstoornissen NGS Epilepsie NGS Hypothyreodie NGS Intellectual disability NGS Mendelioom NGS Wittestofziekten |
