G52W (p.Gly52Trp) variant of RAMP1 (O60894)
G52W (p.Gly52Trp) in RAMP1 (O60894) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G52W (p.Gly52Trp) variant details
- p.Gly52Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available