Allele Registry

Canonical Allele Identifier: PA2827790334

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180811

ClinVar Variation:

189858

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Met146Arg	CA303122 NM_001353961.2:c.437T>G