Allele Registry

Canonical Allele Identifier: PA2826260618

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV003752662

ClinVar Variation:

2864086

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Trp1812Leu	CA349067586 NM_001202435.3:c.5435G>T