Canonical Allele Identifier: PA277499
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67667
ClinVar RCV Id: RCV000058429 RCV000196670 RCV000239767 RCV000656174 RCV001842283
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg523Cys
CA014976
NM_000335.5:c.1567C>T