Canonical Allele Identifier: PA2826976332
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2586722
ClinVar RCV Id: RCV003341793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304947.1:p.Leu165Pro
CA382715505
NM_001318018.2:c.494T>C