Canonical Allele Identifier: PA2825490475
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 532081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Cys1575Tyr
CA352143758
NM_001099404.2:c.4724G>A