Canonical Allele Identifier: PA2826976377
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1284381
ClinVar RCV Id: RCV001699853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304947.1:p.Leu202Pro
CA382714997
NM_001318018.2:c.605T>C