| Approved symbol | SLC39A13 |
|---|---|
| Approved name | solute carrier family 39 member 13 |
| HGCN ID | HGNC:20859 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608735 |
| Chromosome | 11p11.2 |
| Panel(s) |
NGS Ehlers-Danlos syndromes NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Skeletal Dysplasia |
