G58C (p.Gly58Cys) variant of FH (P07954)
G58C (p.Gly58Cys) in FH (P07954) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G58C (p.Gly58Cys) variant details
- p.Gly58Cys
- TOPMed rs11545659
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available