Allele Registry

Canonical Allele Identifier: PA2827790700

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000414318

ClinVar Variation:

372740

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Pro1041Leu	CA16042429 NM_001353961.2:c.3122C>T