Allele Registry

Canonical Allele Identifier: PA2825187118

Gene: APOC2 HGNC NCBI

ClinVar RCV:

RCV004417826

ClinVar Variation:

3127993

HGVS (amino-acid)	Matching Registered Transcripts
NP_000474.2:p.Ala66Pro	CA406294671 NM_000483.5:c.196G>C