Canonical Allele Identifier: PA2827923489
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1411956
ClinVar RCV Id: RCV001923003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ala1561Ser
CA352143725
NM_001354701.2:c.4681G>T