Canonical Allele Identifier: PA2828361651
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1750018
ClinVar RCV Id: RCV002353285 RCV003389906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Tyr1906Cys
CA384889830
NM_001369788.1:c.5717A>G