Canonical Allele Identifier: PA2825025860
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3127887
ClinVar RCV Id: RCV004417720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000030.1:p.Pro27Ser
CA6289903
NM_000039.3:c.79C>T