G66S (p.Gly66Ser) variant of SCN1A (P35498)
G66S (p.Gly66Ser) in SCN1A (P35498) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
G66S (p.Gly66Ser) variant details
- p.Gly66Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available