A11V (p.Ala11Val) variant of CALCB (P10092)
A11V (p.Ala11Val) in CALCB (P10092) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A11V (p.Ala11Val) variant details
- p.Ala11Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available