Canonical Allele Identifier: PA916022138
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304947.1:p.Gly50Arg
CA127561
NM_001318018.2:c.148G>C