Canonical Allele Identifier: PA115615
Gene: APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2573
ClinVar RCV Id: RCV000002682 RCV000991188 RCV000974450 RCV001777130 RCV002444415
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000474.2:p.Lys77Gln
CA115614
NM_000483.5:c.229A>C