Canonical Allele Identifier: PA645417989
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 302506
ClinVar RCV Id: RCV000278412 RCV000396000 RCV002436142 RCV001269105 RCV001859797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000030.1:p.Phe95Tyr
CA6289832
NM_000039.3:c.284T>A