Allele Registry

Canonical Allele Identifier: PA2826130022

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000585876

RCV002248807

ClinVar Variation:

495260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Ala874Thr	CA384887219 NM_001177984.2:c.2620G>A