Allele Registry

Canonical Allele Identifier: PA107505

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059405

RCV000723903

RCV001476333

RCV001836728

ClinVar Variation:

68532

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Glu1238Asp	CA234849 NM_001165963.4:c.3714A>C CA349054671 NM_001165963.4:c.3714A>T