Allele Registry

Canonical Allele Identifier: PA2826260522

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059442

ClinVar Variation:

68567

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Gly1762Glu	CA285012 NM_001202435.3:c.5285G>A