Canonical Allele Identifier: PA093519
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 162015
ClinVar RCV Id: RCV000149436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg223Gly
CA174955
NM_014191.4:c.667A>G