A18D (p.Ala18Asp) variant of CDKN1B (P46527)
A18D (p.Ala18Asp) in CDKN1B (P46527) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
A18D (p.Ala18Asp) variant details
- p.Ala18Asp
- Ensembl rs1277429969
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available