Canonical Allele Identifier: PA2580117973
Gene: APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1744708
ClinVar RCV Id: RCV002343058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000474.2:p.Gly2Arg
CA406291474
NM_000483.5:c.4G>C