Canonical Allele Identifier: PA2825944876
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val1286Ile
CA017761
NM_001160161.2:c.3856G>A