G27R (p.Gly27Arg) variant of FH (P07954)
G27R (p.Gly27Arg) in FH (P07954) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G27R (p.Gly27Arg) variant details
- p.Gly27Arg
- NCI-TCGA TCGA novel
- Ensembl rs2147926940
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available