G27D (p.Gly27Asp) variant of FH (P07954)
G27D (p.Gly27Asp) in FH (P07954) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G27D (p.Gly27Asp) variant details
- p.Gly27Asp
- gnomAD rs1339215584
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available