Allele Registry

Canonical Allele Identifier: PA2827771869

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001070909

ClinVar Variation:

863847

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Pro1737Arg	CA349068404 NM_001353951.2:c.5210C>G