Canonical Allele Identifier: PA2825497281
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1303567
ClinVar RCV Id: RCV001763025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ile1830_Cys1832del
CA2573052150
NM_001099405.2:c.5490_5498del