Canonical Allele Identifier: PA2827922941
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2850307
ClinVar RCV Id: RCV003688243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Cys1197Arg
CA352138139
NM_001354701.2:c.3589T>C