Canonical Allele Identifier: PA2826130826
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1001013
ClinVar RCV Id: RCV001297235
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg1871Lys
CA6571947
NM_001177984.2:c.5612G>A