F88= variant of F13B (Coagulation factor XIII B chain)
F88= in F13B (Coagulation factor XIII B chain) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; low impact. The record also includes structural context.
F88= variant details
- NCI-TCGA Cosmic COSV6637
- Variant assessed as somatic; low impact.
- Missense
- UniProt: Variant assessed as somatic; low impact.
- Structural context available