| Approved symbol | SLC35B2 |
|---|---|
| Approved name | solute carrier family 35 member B2 |
| HGCN ID | HGNC:16872 |
| Previous symbols | |
| Inheritance | |
| OMIM | 610788 |
| Chromosome | 6p21.1 |
| Panel(s) |
NGS Mendeliome NGS White matter disease |
| Approved symbol | SLC35B2 |
|---|---|
| Approved name | solute carrier family 35 member B2 |
| HGCN ID | HGNC:16872 |
| Previous symbols | |
| Inheritance | |
| OMIM | 610788 |
| Chromosome | 6p21.1 |
| Panel(s) |
NGS Mendeliome NGS White matter disease |