Canonical Allele Identifier: PA2825537887
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3069670
ClinVar RCV Id: RCV004008214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Lys442Gln
CA352148353
NM_001099404.2:c.1324A>C