Allele Registry

Canonical Allele Identifier: PA303561

Gene: SCN1A HGNC NCBI

ClinVar Allele:

187787

ClinVar RCV:

RCV000180972

RCV002515213

ClinVar Variation:

190016

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Gly968Glu	CA303559 NM_006920.6:c.2903G>A