Canonical Allele Identifier: PA2826976189
Gene: APOA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17909
ClinVar RCV Id: RCV000019498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304946.1:p.Arg197Cys
CA127537
NM_001318017.2:c.589C>T