Allele Registry

Canonical Allele Identifier: PA2580240486

Gene: AGT HGNC NCBI

ClinVar RCV:

RCV002602413

ClinVar Variation:

2175735

HGVS (amino-acid)	Matching Registered Transcripts
NP_001371408.1:p.Val273Ile	CA1448219 NM_001384479.1:c.817G>A