Allele Registry

Canonical Allele Identifier: PA2826130588

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV003752670

ClinVar Variation:

2864798

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Lys1591Asn	CA384880462 NM_001177984.2:c.4773A>C CA384880463 NM_001177984.2:c.4773A>T