Allele Registry

Canonical Allele Identifier: PA317212

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188864

RCV001528187

RCV001857645

ClinVar Variation:

206761

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Tyr426Cys	CA317209 NM_006920.6:c.1277A>G