Canonical Allele Identifier: PA2826976334
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2866850
ClinVar RCV Id: RCV003700430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304947.1:p.Ser166Gly
CA382715500
NM_001318018.2:c.496A>G