R19W (p.Arg19Trp) variant of KRT12 (Keratin, type I cytoskeletal 12)
R19W (p.Arg19Trp) in KRT12 (Keratin, type I cytoskeletal 12) is a missense change. The available record places it in the context of not provided. The record also includes population frequency data and structural context.
R19W (p.Arg19Trp) variant details
- p.Arg19Trp
- rs200258980
- 1000Genomes rs200258980
- ExAC rs200258980
- TOPMed rs200258980
- not provided
- Missense
- ClinVar: not provided (not provided)
- UniProt: Not provided
- Population evidence available
- Structural context available