Allele Registry

Canonical Allele Identifier: PA2828361210

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000685228

ClinVar Variation:

565622

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Asn1425Ser	CA384908570 NM_001369788.1:c.4274A>G