Canonical Allele Identifier: PA2826130732
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 579919
ClinVar RCV Id: RCV000703318 RCV000763861 RCV002343547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ile1786Val
CA6571922
NM_001177984.2:c.5356A>G