Canonical Allele Identifier: PA177805
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67769
ClinVar RCV Id: RCV000058539 RCV000151788 RCV000845398 RCV001149576 RCV000724184 RCV000852549 RCV001149577 RCV001149579 RCV001149578 RCV001149580 RCV001145287 RCV001842322 RCV002433564 RCV004537260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Cys982Arg
CA016652
NM_000335.5:c.2944T>C