| Approved symbol | VWA3B |
|---|---|
| Approved name | von Willebrand factor A domain containing 3B |
| HGCN ID | HGNC:28385 |
| Previous symbols | |
| Inheritance | |
| OMIM | 614884 |
| Chromosome | 2q11.2 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) |
