Canonical Allele Identifier: PA2826130339
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1471659
ClinVar RCV Id: RCV001966886
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Met1287Val
CA384904591
NM_001177984.2:c.3859A>G