Canonical Allele Identifier: PA2825537694
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1171664
ClinVar RCV Id: RCV001842101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.His278Tyr
CA352150599
NM_001099404.2:c.832C>T