Allele Registry

Canonical Allele Identifier: PA2828361400

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV001775251

ClinVar Variation:

1320078

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Ala1609Asp	CA384880650 NM_001369788.1:c.4826C>A