Allele Registry

Canonical Allele Identifier: PA2827771998

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003754652

ClinVar Variation:

2846763

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Asp1805Glu	CA349067509 NM_001353951.2:c.5415T>G CA349067511 NM_001353951.2:c.5415T>A