| Approved symbol | SLC52A3 |
|---|---|
| Approved name | solute carrier family 52 member 3 |
| HGCN ID | HGNC:16187 |
| Previous symbols | C20orf54 |
| Inheritance | |
| OMIM | 613350 |
| Chromosome | 20p13 |
| Panel(s) |
NGS Fetal akinesia deformation sequence FADS NGS Mendeliome NGS Movement disorders NGS Muscle disorders NGS Neuropathy/Charcot Marie Tooth NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders |
