Canonical Allele Identifier: PA2825490985
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1524388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Phe1752del
CA2580614204
NM_001099404.2:c.5254_5256del