Canonical Allele Identifier: PA2826130551
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1347532
ClinVar RCV Id: RCV002041744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ile1565Thr
CA384880302
NM_001177984.2:c.4694T>C