F42C (p.Phe42Cys) variant of F13B (Coagulation factor XIII B chain)
F42C (p.Phe42Cys) 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.
F42C (p.Phe42Cys) variant details
- p.Phe42Cys
- NCI-TCGA Cosmic COSV6637
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available