Allele Registry

Canonical Allele Identifier: PA2827785653

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001229261

RCV001311216

ClinVar Variation:

206797

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Asp1046Asn	CA317351 NM_001353958.2:c.3136G>A