Allele Registry

Canonical Allele Identifier: PA2828932764

Gene: AGT HGNC NCBI

ClinVar RCV:

RCV002602413

ClinVar Variation:

2175735

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369746.2:p.Val273Ile	CA1448219 NM_001382817.3:c.817G>A