Canonical Allele Identifier: PA2825492371
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1749427
ClinVar RCV Id: RCV002349919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Pro192Thr
CA352153651
NM_001099405.2:c.574C>A