Canonical Allele Identifier: PA2826976196
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1284381
ClinVar RCV Id: RCV001699853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Leu202Pro
CA382714997
NM_001318017.2:c.605T>C