Canonical Allele Identifier: PA2825025995
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2866850
ClinVar RCV Id: RCV003700430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000030.1:p.Ser166Gly
CA382715500
NM_000039.3:c.496A>G