E22D (p.Glu22Asp) variant of F13B (Coagulation factor XIII B chain)
E22D (p.Glu22Asp) in F13B (Coagulation factor XIII B chain) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E22D (p.Glu22Asp) variant details
- p.Glu22Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available