Allele Registry

Canonical Allele Identifier: PA2580117975

Gene: APOC2 HGNC NCBI

ClinVar RCV:

RCV002347083

ClinVar Variation:

1747123

HGVS (amino-acid)	Matching Registered Transcripts
NP_000474.2:p.Arg4Gln	CA9506569 NM_000483.5:c.11G>A