Canonical Allele Identifier: PA2825945600
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Tyr1741Cys
CA019196
NM_001160161.2:c.5222A>G