Canonical Allele Identifier: PA2580240477
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 1928642
ClinVar RCV Id: RCV002635076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371408.1:p.Arg165Gln
CA1448285
NM_001384479.1:c.494G>A