Canonical Allele Identifier: PA2825490055
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2875975
ClinVar RCV Id: RCV003707531
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gly1433Arg
CA72943607
NM_001099404.2:c.4297G>A
CA352145548
NM_001099404.2:c.4297G>C