Allele Registry

Canonical Allele Identifier: PA2573169956

Gene: APOC2 HGNC NCBI

ClinVar RCV:

RCV002096391

RCV002372927

ClinVar Variation:

1591835

HGVS (amino-acid)	Matching Registered Transcripts
NP_000474.2:p.Thr3Ile	CA9506565 NM_000483.5:c.8C>T