A120G (p.Ala120Gly) variant of ITGA2B (Integrin alpha-IIb)
A120G (p.Ala120Gly) in ITGA2B (Integrin alpha-IIb) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
A120G (p.Ala120Gly) variant details
- p.Ala120Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available