Canonical Allele Identifier: PA2828361241
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 280470
ClinVar RCV Id: RCV000338932 RCV000636327 RCV001254990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Met1440Val
CA10603278
NM_001369788.1:c.4318A>G