Canonical Allele Identifier: PA2826976253
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3127887
ClinVar RCV Id: RCV004417720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304947.1:p.Pro27Ser
CA6289903
NM_001318018.2:c.79C>T