Canonical Allele Identifier: PA2825490542
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1743292
ClinVar RCV Id: RCV002337967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Val1604Ala
CA352143572
NM_001099404.2:c.4811T>C