Allele Registry

Canonical Allele Identifier: PA2828932773

Gene: AGT HGNC NCBI

ClinVar RCV:

RCV001967789

ClinVar Variation:

1440909

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369746.2:p.Arg366Leu	CA345203700 NM_001382817.3:c.1097G>T