Canonical Allele Identifier: PA2827923564
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg1604Gln
CA018670
NM_001354701.2:c.4811G>A