Canonical Allele Identifier: PA2826976141
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17913
ClinVar RCV Id: RCV000019502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Glu160Lys
CA127549
NM_001318017.2:c.478G>A