C13W (p.Cys13Trp) variant of CDKN1A (P38936)
C13W (p.Cys13Trp) in CDKN1A (P38936) is a missense change.
C13W (p.Cys13Trp) variant details
- p.Cys13Trp
- ExAC rs756319938
- TOPMed rs756319938
- gnomAD rs756319938
- Missense
C13W (p.Cys13Trp) in CDKN1A (P38936) is a missense change.