Canonical Allele Identifier: PA2825942136
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2584499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Lys1476Thr
CA352145222
NM_001160160.2:c.4427A>C