V27G (p.Val27Gly) variant of ADH1B (P00325)
V27G (p.Val27Gly) in ADH1B (P00325) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V27G (p.Val27Gly) variant details
- p.Val27Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available