Canonical Allele Identifier: PA2580118010
Gene: APOC2 HGNC NCBI
ClinVar RCV:
RCV003176547
ClinVar Variation:
2447635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000474.2:p.Ser83Thr
CA406295265
NM_000483.5:c.248G>C