Canonical Allele Identifier: PA2825494554
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2689923
ClinVar RCV Id: RCV003491444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ile891Thr
CA060679
NM_001099405.2:c.2672T>C