Canonical Allele Identifier: PA2825494098
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2435760
ClinVar RCV Id: RCV003136510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Arg689Pro
CA352144848
NM_001099405.2:c.2066G>C