Canonical Allele Identifier: PA2826130761
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1464681
ClinVar RCV Id: RCV001979185
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Glu1820Gly
CA384887768
NM_001177984.2:c.5459A>G