C19A (p.Cys19Ala) variant of F2 (Prothrombin)
C19A (p.Cys19Ala) in F2 (Prothrombin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
C19A (p.Cys19Ala) variant details
- p.Cys19Ala
- NCI-TCGA Cosmic COSV6131
- cosmic curated COSV61317
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available