Allele Registry

Canonical Allele Identifier: PA2828360321

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000239739

RCV001054624

ClinVar Variation:

253279

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Phe260Ser	CA10586288 NM_001369788.1:c.779T>C