Canonical Allele Identifier: PA2825945319
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val1570Ile
CA018686
NM_001160161.2:c.4708G>A