D59H (p.Asp59His) variant of ITGA2B (Integrin alpha-IIb)
D59H (p.Asp59His) in ITGA2B (Integrin alpha-IIb) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D59H (p.Asp59His) variant details
- p.Asp59His
- NCI-TCGA Cosmic COSV9928
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available