Allele Registry

Canonical Allele Identifier: PA2741818270

Gene: APOC2 HGNC NCBI

ClinVar RCV:

RCV003377764

ClinVar Variation:

2625085

HGVS (amino-acid)	Matching Registered Transcripts
NP_000474.2:p.Pro65Ser	CA406294639 NM_000483.5:c.193C>T