Canonical Allele Identifier: PA2826976079
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1500563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Ser79Phe
CA382717361
NM_001318017.2:c.236C>T