Allele Registry

Canonical Allele Identifier: PA658829061

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000658882

ClinVar Variation:

546874

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Trp1801Cys	CA349067580 NM_006920.6:c.5403G>T CA349067582 NM_006920.6:c.5403G>C