Canonical Allele Identifier: PA2828452057
Gene: APOA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 4403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358833.1:p.Ser19Trp
CA116845
NM_001371904.1:c.56C>G