Allele Registry

Canonical Allele Identifier: PA2827760117

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000472521

ClinVar Variation:

408936

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Leu1412Val	CA16610151 NM_001353949.2:c.4234C>G