Allele Registry

Canonical Allele Identifier: PA2826260456

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000530416

ClinVar Variation:

461280

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Gly1725Asp	CA349068786 NM_001202435.3:c.5174G>A