Allele Registry

Canonical Allele Identifier: PA2827786885

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003752662

ClinVar Variation:

2864086

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Trp1784Leu	CA349067586 NM_001353958.2:c.5351G>T