D17H (p.Asp17His) variant of CDKN1B (P46527)
D17H (p.Asp17His) in CDKN1B (P46527) is a missense change. The record also includes structural context.
D17H (p.Asp17His) variant details
- p.Asp17His
- Ensembl rs2136355436
- Missense
- Structural context available