| Approved symbol | SLC38A8 |
|---|---|
| Approved name | solute carrier family 38 member 8 |
| HGCN ID | HGNC:32434 |
| Previous symbols | |
| Inheritance | |
| OMIM | 615585 |
| Chromosome | 16q23.3 |
| Panel(s) |
NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Vision disorder Albinism |
