Canonical Allele Identifier: PA2827921977
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Thr559Ile
CA015154
NM_001354701.2:c.1676C>T