F27V (p.Phe27Val) variant of RARA (Retinoic acid receptor alpha)
F27V (p.Phe27Val) in RARA (Retinoic acid receptor alpha) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F27V (p.Phe27Val) variant details
- p.Phe27Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available