Canonical Allele Identifier: PA2825026017
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1907392
ClinVar RCV Id: RCV002578207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000030.1:p.His179Gln
CA382715294
NM_000039.3:c.537T>G
CA382715295
NM_000039.3:c.537T>A