Canonical Allele Identifier: PA2825538143
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 922452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Cys649Tyr
CA352145106
NM_001099404.2:c.1946G>A