Canonical Allele Identifier: PA2573169956
Gene: APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1591835
ClinVar RCV Id: RCV002096391 RCV002372927
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Amino-acid Alleles

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