Allele Registry

Canonical Allele Identifier: PA2828361259

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000441856

ClinVar Variation:

377169

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Gln1460Lys	CA16603287 NM_001369788.1:c.4378C>A