Allele Registry

Canonical Allele Identifier: PA2580118015

Gene: APOC2 HGNC NCBI

ClinVar RCV:

RCV003165341

ClinVar Variation:

2447633

HGVS (amino-acid)	Matching Registered Transcripts
NP_000474.2:p.Thr86Arg	CA9506646 NM_000483.5:c.257C>G