Canonical Allele Identifier: PA2827922936
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1702737
ClinVar RCV Id: RCV002279055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Leu1193Trp
CA352138161
NM_001354701.2:c.3578T>G