Canonical Allele Identifier: PA2826976090
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1513939
ClinVar RCV Id: RCV002018517 RCV002498049
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Val91Leu
CA382717089
NM_001318017.2:c.271G>T
CA382717092
NM_001318017.2:c.271G>C