Canonical Allele Identifier: PA2825942306
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Val1591Ile
CA018686
NM_001160160.2:c.4771G>A