Allele Registry

Canonical Allele Identifier: PA2827771990

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003752662

ClinVar Variation:

2864086

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Trp1801Leu	CA349067586 NM_001353951.2:c.5402G>T