Canonical Allele Identifier: PA2827921945
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1171660
ClinVar RCV Id: RCV001842099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Phe543Ser
CA352147095
NM_001354701.2:c.1628T>C