N36T (p.Asn36Thr) variant of SCN1A (P35498)
N36T (p.Asn36Thr) 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.
N36T (p.Asn36Thr) variant details
- p.Asn36Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available