Allele Registry

Canonical Allele Identifier: PA2828932776

Gene: AGT HGNC NCBI

ClinVar RCV:

RCV002110308

ClinVar Variation:

1623773

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369746.2:p.Ala394dup	CA1448100 NM_001382817.3:c.1180_1182dup