G131C (p.Gly131Cys) variant of VWF (von Willebrand factor)
G131C (p.Gly131Cys) in VWF (von Willebrand factor) is a missense change. Clinical records from EBI and UniProt describe it as benign. The record also includes structural context.
G131C (p.Gly131Cys) variant details
- p.Gly131Cys
- 1000Genomes rs76505074
- ESP rs76505074
- ExAC rs76505074
- TOPMed rs76505074
- Benign
- Missense
- EBI: Benign
- UniProt: Benign
- Structural context available