Canonical Allele Identifier: PA113496
Gene: APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000474.2:p.Trp48Arg
CA115625
NM_000483.5:c.142T>C
CA406294259
NM_000483.5:c.142T>A