| Approved symbol | SLC19A2 |
|---|---|
| Approved name | solute carrier family 19 member 2 |
| HGCN ID | HGNC:10938 |
| Previous symbols | TRMA |
| Inheritance | |
| OMIM | 603941 |
| Chromosome | 1q24.2 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Neonatal diabetes mellitus NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
