Allele Registry

Canonical Allele Identifier: PA2826011433

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000518488

ClinVar Variation:

448251

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Arg101Leu	CA349077140 NM_001165964.3:c.302G>T