A76D (p.Ala76Asp) variant of PDGFRB (P09619)
A76D (p.Ala76Asp) in PDGFRB (P09619) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A76D (p.Ala76Asp) variant details
- p.Ala76Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available