R34G (p.Arg34Gly) variant of KRT2 (P35908)
R34G (p.Arg34Gly) in KRT2 (P35908) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes population frequency data and structural context.
R34G (p.Arg34Gly) variant details
- p.Arg34Gly
- 1000Genomes rs35460418
- ESP rs35460418
- ExAC rs35460418
- TOPMed rs35460418
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Population evidence available
- Structural context available