L11P (p.Leu11Pro) variant of ITGA2B (Integrin alpha-IIb)
L11P (p.Leu11Pro) 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.
L11P (p.Leu11Pro) variant details
- p.Leu11Pro
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available