Canonical Allele Identifier: PA2825944398
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg986Trp
CA016660
NM_001160161.2:c.2956C>T