Canonical Allele Identifier: PA2826976093
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3231915
ClinVar RCV Id: RCV004518630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Gln93His
CA382717037
NM_001318017.2:c.279G>T
CA382717040
NM_001318017.2:c.279G>C