F26V (p.Phe26Val) variant of PRPH2 (Peripherin-2)
F26V (p.Phe26Val) in PRPH2 (Peripherin-2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F26V (p.Phe26Val) variant details
- p.Phe26Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available