Canonical Allele Identifier: PA2826976150
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2642398
ClinVar RCV Id: RCV003398147

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Lys164Arg
CA382715522
NM_001318017.2:c.491A>G