Canonical Allele Identifier: PA2827923567
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Val1605Ile
CA018686
NM_001354701.2:c.4813G>A