Allele Registry

Canonical Allele Identifier: PA2573205708

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001971003

ClinVar Variation:

1474062

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Thr844Ser	CA349069931 NM_001353961.2:c.2530A>T