Canonical Allele Identifier: PA2826976441
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2642398
ClinVar RCV Id: RCV003398147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304950.1:p.Lys55Arg
CA382715522
NM_001318021.1:c.164A>G