| Approved symbol | SLC1A4 |
|---|---|
| Approved name | solute carrier family 1 member 4 |
| HGCN ID | HGNC:10942 |
| Previous symbols | |
| Inheritance | |
| OMIM | 600229 |
| Chromosome | 2p14 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Microcephaly NGS Preconception panel (for consanguineous couples) NGS White matter disease |
