G66V (p.Gly66Val) variant of SCN1A (P35498)
G66V (p.Gly66Val) in SCN1A (P35498) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G66V (p.Gly66Val) variant details
- p.Gly66Val
- NCI-TCGA Cosmic COSV5768
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available