Canonical Allele Identifier: PA2825491400
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1748932
ClinVar RCV Id: RCV002347332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser1888del
CA2580069737
NM_001099404.2:c.5663_5665del