Allele Registry

Canonical Allele Identifier: PA2828361235

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV001224613

ClinVar Variation:

952494

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Ile1438Leu	CA384909033 NM_001369788.1:c.4312A>C