A57G (p.Ala57Gly) variant of SCN1A (P35498)
A57G (p.Ala57Gly) 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.
A57G (p.Ala57Gly) variant details
- p.Ala57Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available