S13C (p.Ser13Cys) variant of KRT17 (Keratin, type I cytoskeletal 17)
S13C (p.Ser13Cys) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The record also includes structural context.
S13C (p.Ser13Cys) variant details
- p.Ser13Cys
- 1000Genomes rs2144617152
- Missense
- Structural context available