Canonical Allele Identifier: PA2825940733
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Thr559Ile
CA015154
NM_001160160.2:c.1676C>T