Canonical Allele Identifier: PA2825944002
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 532115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Tyr694Cys
CA352144821
NM_001160161.2:c.2081A>G