Canonical Allele Identifier: PA2825537601
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 924054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Thr169Asn
CA352153939
NM_001099404.2:c.506C>A