Canonical Allele Identifier: PA2573198581
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1410343
ClinVar RCV Id: RCV001940062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304947.1:p.Arg19Trp
CA6289907
NM_001318018.2:c.55C>T