Canonical Allele Identifier: PA307728
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67934
ClinVar RCV Id: RCV000058718 RCV000183089 RCV000252940 RCV000779405 RCV001842372
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg1625His
CA018698
NM_000335.5:c.4874G>A