Canonical Allele Identifier: PA2827922804
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Asp1113Asn
CA017057
NM_001354701.2:c.3337G>A