Canonical Allele Identifier: PA330232
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67981
ClinVar RCV Id: RCV000058767
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Leu1772Val
CA019110
NM_001099404.2:c.5314C>G