Canonical Allele Identifier: PA2828361640
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1516886
ClinVar RCV Id: RCV002026928
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1891Gln
CA6571956
NM_001369788.1:c.5672G>A