Canonical Allele Identifier: PA2825496607
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Val1606Ile
CA018686
NM_001099405.2:c.4816G>A