Canonical Allele Identifier: PA2825944137
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1790960
ClinVar RCV Id: RCV002450374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val806Gly
CA352143212
NM_001160161.2:c.2417T>G