Allele Registry

Canonical Allele Identifier: PA2580117973

Gene: APOC2 HGNC NCBI

ClinVar RCV:

RCV002343058

ClinVar Variation:

1744708

HGVS (amino-acid)	Matching Registered Transcripts
NP_000474.2:p.Gly2Arg	CA406291474 NM_000483.5:c.4G>C