Allele Registry

Canonical Allele Identifier: PA2827771828

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000530416

ClinVar Variation:

461280

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Gly1714Asp	CA349068786 NM_001353951.2:c.5141G>A