Allele Registry

Canonical Allele Identifier: PA2829676552

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003752662

ClinVar Variation:

2864086

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Trp1801Leu	CA349067586 NM_006920.6:c.5402G>T