Canonical Allele Identifier: PA2825496192
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2584499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Lys1459Thr
CA352145222
NM_001099405.2:c.4376A>C