Canonical Allele Identifier: PA2826130705
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2505215
ClinVar RCV Id: RCV003233392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Phe1747Val
CA384885545
NM_001177984.2:c.5239T>G