Canonical Allele Identifier: PA2825491502
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 75052
ClinVar RCV Id: RCV001842422 RCV003539789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg1929Cys
CA064797
NM_001099404.2:c.5785C>T