G21A (p.Gly21Ala) variant of CALCB (P10092)
G21A (p.Gly21Ala) 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.
G21A (p.Gly21Ala) variant details
- p.Gly21Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available