| Approved symbol | SLC13A5 |
|---|---|
| Approved name | solute carrier family 13 member 5 |
| HGCN ID | HGNC:23089 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608305 |
| Chromosome | 17p13.1 |
| Panel(s) |
NGS Epilepsie NGS Intellectual disability NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) |
