Canonical Allele Identifier: PA2580118004
Gene: APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1928114
ClinVar RCV Id: RCV002614367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000474.2:p.Ala80Thr
CA406295197
NM_000483.5:c.238G>A