Canonical Allele Identifier: PA2825941342
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67770

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Arg986Gln
CA016672
NM_001160160.2:c.2957G>A