Canonical Allele Identifier: PA2828361536
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 954719
ClinVar RCV Id: RCV001227231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1800Pro
CA384887140
NM_001369788.1:c.5399G>C