Canonical Allele Identifier: PA115622
Gene: APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2581
ClinVar RCV Id: RCV000002697 RCV001135899 RCV001551048 RCV003162207 RCV003904797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000474.2:p.Lys41Thr
CA115621
NM_000483.5:c.122A>C