R32G (p.Arg32Gly) variant of CDKN1A (P38936)
R32G (p.Arg32Gly) in CDKN1A (P38936) is a missense change. The record also includes structural context.
R32G (p.Arg32Gly) variant details
- p.Arg32Gly
- ESP rs373450720
- ExAC rs373450720
- TOPMed rs373450720
- gnomAD rs373450720
- Missense
- Structural context available