G69D (p.Gly69Asp) variant of ITGA2B (Integrin alpha-IIb)
G69D (p.Gly69Asp) in ITGA2B (Integrin alpha-IIb) is a missense change. The record also includes structural context.
G69D (p.Gly69Asp) variant details
- p.Gly69Asp
- Ensembl rs2048647129
- Missense
- Structural context available