Allele Registry

Canonical Allele Identifier: PA2827783921

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000658882

ClinVar Variation:

546874

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Trp1784Cys	CA349067580 NM_001353957.2:c.5352G>T CA349067582 NM_001353957.2:c.5352G>C