S27C (p.Ser27Cys) variant of CDKN1A (P38936)
S27C (p.Ser27Cys) in CDKN1A (P38936) is a missense change. The record also includes structural context.
S27C (p.Ser27Cys) variant details
- p.Ser27Cys
- ExAC rs775222810
- TOPMed rs775222810
- gnomAD rs775222810
- Missense
- Structural context available