Canonical Allele Identifier: PA2580118023
Gene: APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2447634
ClinVar RCV Id: RCV003165342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000474.2:p.Gly99Glu
CA406295499
NM_000483.5:c.296G>A