Allele Registry

Canonical Allele Identifier: PA303562

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180972

RCV002515213

ClinVar Variation:

190016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Gly979Glu	CA303559 NM_001165963.4:c.2936G>A