Canonical Allele Identifier: PA2825026019
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1341582
ClinVar RCV Id: RCV001837078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000030.1:p.Asp181Gly
CA382715274
NM_000039.3:c.542A>G