Canonical Allele Identifier: PA2828360756
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 309354
ClinVar RCV Id: RCV000312849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Tyr811Cys
CA10633090
NM_001369788.1:c.2432A>G