R37G (p.Arg37Gly) variant of KRT1 (Keratin, type II cytoskeletal 1)
R37G (p.Arg37Gly) in KRT1 (Keratin, type II cytoskeletal 1) is a missense change. The record also includes structural context.
R37G (p.Arg37Gly) variant details
- p.Arg37Gly
- ExAC rs769301639
- TOPMed rs769301639
- gnomAD rs769301639
- Missense
- Structural context available