Canonical Allele Identifier: PA2826130775
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1505439
ClinVar RCV Id: RCV001999506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Met1828Val
CA384887974
NM_001177984.2:c.5482A>G