Allele Registry

Canonical Allele Identifier: PA2828361380

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000488921

ClinVar Variation:

427167

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Ile1590Asn	CA384880452 NM_001369788.1:c.4769T>A