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 Bewegingsstoornissen NGS Intellectual disability NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) |