Canonical Allele Identifier: PA2825942584
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Tyr1762Cys
CA019196
NM_001160160.2:c.5285A>G