Canonical Allele Identifier: PA2828361666
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2444693
ClinVar RCV Id: RCV003154141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1930Gly
CA384890509
NM_001369788.1:c.5788A>G