Allele Registry

Canonical Allele Identifier: PA2827789176

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059510

RCV001091662

RCV001253411

RCV001328668

RCV001507578

RCV001854245

ClinVar Variation:

68631

1027787

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Trp1405Arg	CA285165 NM_001353960.2:c.4213T>C CA349049615 NM_001353960.2:c.4213T>A