Canonical Allele Identifier: PA2828360705
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 945997
ClinVar RCV Id: RCV001216764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Cys722Trp
CA384879757
NM_001369788.1:c.2166C>G