A138D (p.Ala138Asp) variant of VWF (von Willebrand factor)
A138D (p.Ala138Asp) in VWF (von Willebrand factor) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A138D (p.Ala138Asp) variant details
- p.Ala138Asp
- rs932271358
- NCI-TCGA Cosmic COSV9978
- TOPMed rs932271358
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available