Allele Registry

Canonical Allele Identifier: PA2828361233

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000239737

ClinVar Variation:

207120

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Ile1438Val	CA318278 NM_001369788.1:c.4312A>G