L79M (p.Leu79Met) variant of KRT17 (Keratin, type I cytoskeletal 17)
L79M (p.Leu79Met) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The record also includes structural context.
L79M (p.Leu79Met) variant details
- p.Leu79Met
- TOPMed rs1028399478
- gnomAD rs1028399478
- Missense
- Structural context available