Allele Registry

Canonical Allele Identifier: PA916036788

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188945

RCV003753104

ClinVar Variation:

206822

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Ala615Thr	CA317442 NM_001353961.2:c.1843G>A