Canonical Allele Identifier: PA2825128775
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1171664
ClinVar RCV Id: RCV001842101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.His278Tyr
CA352150599
NM_000335.5:c.832C>T