Allele Registry

Canonical Allele Identifier: PA2826129478

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000413127

RCV000699586

ClinVar Variation:

373565

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Val211Ala	CA16042901 NM_001177984.2:c.632T>C