G56D (p.Gly56Asp) variant of PDGFRB (P09619)
G56D (p.Gly56Asp) in PDGFRB (P09619) is a missense change. The record also includes structural context.
G56D (p.Gly56Asp) variant details
- p.Gly56Asp
- TOPMed rs1760610944
- Missense
- Structural context available