P11S (p.Pro11Ser) variant of SCN4A (Nav1.4)
P11S (p.Pro11Ser) in SCN4A (Nav1.4) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P11S (p.Pro11Ser) variant details
- p.Pro11Ser
- NCI-TCGA Cosmic COSV1014
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available