Allele Registry

Canonical Allele Identifier: PA2828361381

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000851494

RCV001858503

ClinVar Variation:

691254

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Ile1590Thr	CA384880453 NM_001369788.1:c.4769T>C