W139C (p.Trp139Cys) variant of KRT13 (Keratin, type I cytoskeletal 13)
W139C (p.Trp139Cys) in KRT13 (Keratin, type I cytoskeletal 13) is a missense change. The record also includes structural context.
W139C (p.Trp139Cys) variant details
- p.Trp139Cys
- gnomAD rs1447201597
- Missense
- Structural context available