R43C (p.Arg43Cys) variant of LHCGR (P22888)
R43C (p.Arg43Cys) in LHCGR (P22888) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R43C (p.Arg43Cys) variant details
- p.Arg43Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available