S79G (p.Ser79Gly) variant of KRT14 (Keratin, type I cytoskeletal 14)
S79G (p.Ser79Gly) in KRT14 (Keratin, type I cytoskeletal 14) is a missense change. The record also includes structural context.
S79G (p.Ser79Gly) variant details
- p.Ser79Gly
- gnomAD rs1907538490
- Missense
- Structural context available