Allele Registry

Canonical Allele Identifier: PA2826258798

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV002314381

ClinVar Variation:

588285

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ser626Cys	CA349067383 NM_001202435.3:c.1876A>T