Canonical Allele Identifier: PA2825941562
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asp1113Asn
CA017057
NM_001160160.2:c.3337G>A