Allele Registry

Canonical Allele Identifier: PA317444

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188945

RCV003753104

ClinVar Variation:

206822

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Ala1418Thr	CA317442 NM_006920.6:c.4252G>A