Allele Registry

Canonical Allele Identifier: PA2826260830

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001200251

RCV001318625

ClinVar Variation:

206732

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ile1955Met	CA317108 NM_001202435.3:c.5865A>G