D26G (p.Asp26Gly) variant of CDKN1A (P38936)
D26G (p.Asp26Gly) in CDKN1A (P38936) is a missense change. The record also includes structural context.
D26G (p.Asp26Gly) variant details
- p.Asp26Gly
- Ensembl rs2150312957
- Missense
- Structural context available