Canonical Allele Identifier: PA2826976190
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2137255
ClinVar RCV Id: RCV003062459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Arg197Pro
CA229324102
NM_001318017.2:c.590G>C