Canonical Allele Identifier: PA127529
Gene: APOC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 17902
ClinVar RCV Id: RCV000019491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000031.1:p.Thr94Ala
CA127528
NM_000040.3:c.280A>G