Canonical Allele Identifier: PA2826129491
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 162015
ClinVar RCV Id: RCV000149436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg223Gly
CA174955
NM_001177984.2:c.667A>G