P56H (p.Pro56His) variant of FBN1 (Fibrillin-1)
P56H (p.Pro56His) in FBN1 (Fibrillin-1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P56H (p.Pro56His) variant details
- p.Pro56His
- NCI-TCGA Cosmic COSV1003
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.