Canonical Allele Identifier: PA2825128854
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1766358
ClinVar RCV Id: RCV002450072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ser309Cys
CA352150332
NM_000335.5:c.925A>T