Canonical Allele Identifier: PA116846
Gene: APOA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 4403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443200.2:p.Ser19Trp
CA116845
NM_052968.5:c.56C>G