Allele Registry

Canonical Allele Identifier: PA317151

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188840

RCV003448282

ClinVar Variation:

206745

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Leu221Pro	CA317148 NM_006920.6:c.662T>C