Canonical Allele Identifier: PA2827290854
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1031970
ClinVar RCV Id: RCV001333926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Arg226Gly
CA385224768
NM_001330260.2:c.676C>G