Canonical Allele Identifier: PA2826976213
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 878622
ClinVar RCV Id: RCV001105370 RCV001105371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Thr226Met
CA382714518
NM_001318017.2:c.677C>T