F91C (p.Phe91Cys) variant of VWF (von Willebrand factor)
F91C (p.Phe91Cys) 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.
F91C (p.Phe91Cys) variant details
- p.Phe91Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available