Allele Registry

Canonical Allele Identifier: PA3057552024

Gene: APOC2 HGNC NCBI

ClinVar RCV:

RCV004653723

ClinVar Variation:

3308437

HGVS (amino-acid)	Matching Registered Transcripts
NP_000474.2:p.Lys77Arg	CA406295146 NM_000483.5:c.230A>G