Canonical Allele Identifier: PA2827923252
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Val1404Met
CA017946
NM_001354701.2:c.4210G>A