S66N (p.Ser66Asn) variant of KRT12 (Keratin, type I cytoskeletal 12)
S66N (p.Ser66Asn) in KRT12 (Keratin, type I cytoskeletal 12) is a missense change. The record also includes structural context.
S66N (p.Ser66Asn) variant details
- p.Ser66Asn
- 1000Genomes rs202056647
- ExAC rs202056647
- TOPMed rs202056647
- gnomAD rs202056647
- Missense
- Structural context available