Allele Registry

Canonical Allele Identifier: PA645449020

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000413127

RCV000699586

ClinVar Variation:

373565

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Val211Ala	CA16042901 NM_014191.4:c.632T>C