Allele Registry

Canonical Allele Identifier: PA108511

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059510

RCV001091662

RCV001253411

RCV001328668

RCV001507578

RCV001854245

ClinVar Variation:

68631

1027787

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Trp1434Arg	CA285165 NM_001165963.4:c.4300T>C CA349049615 NM_001165963.4:c.4300T>A