Allele Registry

Canonical Allele Identifier: PA317769

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000189076

RCV001060675

ClinVar Variation:

206932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.His324Arg	CA317767 NM_001165963.4:c.971A>G