Canonical Allele Identifier: PA2825538188
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 972689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg693Leu
CA352144827
NM_001099404.2:c.2078G>T