Canonical Allele Identifier: PA264952
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67671
ClinVar RCV Id: RCV000058434 RCV000182979 RCV000490338 RCV001842287 RCV002483110
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Phe532Cys
CA015051
NM_001099404.2:c.1595T>G