E20D (p.Glu20Asp) variant of SCN1A (Nav1.1)
E20D (p.Glu20Asp) in SCN1A (Nav1.1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E20D (p.Glu20Asp) variant details
- p.Glu20Asp
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10032
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available