A29T (p.Ala29Thr) variant of ITGA2B (Integrin alpha-IIb)
A29T (p.Ala29Thr) 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.
A29T (p.Ala29Thr) variant details
- p.Ala29Thr
- NCI-TCGA Cosmic COSV5223
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available