Canonical Allele Identifier: PA265793
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67963
ClinVar RCV Id: RCV000058749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Cys1728Arg
CA018958
NM_001099404.2:c.5182T>C