Canonical Allele Identifier: PA2825130891
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 901139
ClinVar RCV Id: RCV001146836 RCV001146838 RCV001146837 RCV001146839 RCV001146834 RCV001146835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Cys1175Tyr
CA352138276
NM_000335.5:c.3524G>A