Canonical Allele Identifier: PA2825940192
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67991
ClinVar RCV Id: RCV000058781 RCV004546427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Cys182Arg
CA019232
NM_001160160.2:c.544T>C