Canonical Allele Identifier: PA2826976186
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1749121
ClinVar RCV Id: RCV002347521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Tyr190Cys
CA382715175
NM_001318017.2:c.569A>G