Canonical Allele Identifier: PA2828361659
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1042696
ClinVar RCV Id: RCV001346691 RCV004036500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1919Trp
CA236327953
NM_001369788.1:c.5755C>T