Allele Registry

Canonical Allele Identifier: PA2829676388

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001090359

RCV001862677

ClinVar Variation:

870750

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Thr1698Asn	CA349069066 NM_006920.6:c.5093C>A