Y39H (p.Tyr39His) variant of F13B (Coagulation factor XIII B chain)
Y39H (p.Tyr39His) 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.
Y39H (p.Tyr39His) variant details
- p.Tyr39His
- NCI-TCGA Cosmic COSV6637
- Ensembl rs1655923872
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available