Allele Registry

Canonical Allele Identifier: PA2826259926

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414265

ClinVar Variation:

372903

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Gln1427Leu	CA16042437 NM_001202435.3:c.4280A>T