Allele Registry

Canonical Allele Identifier: PA2827762537

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000518488

ClinVar Variation:

448251

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Arg101Leu	CA349077140 NM_001353950.2:c.302G>T