Canonical Allele Identifier: PA2825538298
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1061680
ClinVar RCV Id: RCV003656950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser799Tyr
CA352143259
NM_001099404.2:c.2396C>A