Allele Registry

Canonical Allele Identifier: PA2826012700

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188905

RCV001317116

ClinVar Variation:

206794

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Ala961Val	CA317339 NM_001165964.3:c.2882C>T