Allele Registry

Canonical Allele Identifier: PA2827764864

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000413718

ClinVar Variation:

372972

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Leu858Ser	CA16042442 NM_001353950.2:c.2573T>C