Canonical Allele Identifier: PA284755
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67978
ClinVar RCV Id: RCV000058764 RCV000157474 RCV000212988 RCV000619162 RCV000623091 RCV001146621 RCV000987246 RCV001146622 RCV001146623 RCV001146624 RCV001146625 RCV001842382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg18Trp
CA019099
NM_000335.5:c.52C>T