Canonical Allele Identifier: PA916022152
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17910

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304950.1:p.Pro58Arg
CA127540
NM_001318021.1:c.173C>G