Canonical Allele Identifier: PA2580180235
Gene: APOM HGNC NCBI

Linked Data

ClinVar Variation Id: 2337233
ClinVar RCV Id: RCV004176000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243098.1:p.Glu83Lys
CA3718031
NM_001256169.2:c.247G>A