Allele Registry

Canonical Allele Identifier: PA2573216563

Gene: AGT HGNC NCBI

ClinVar RCV:

RCV002110308

ClinVar Variation:

1623773

HGVS (amino-acid)	Matching Registered Transcripts
NP_001371408.1:p.Ala394dup	CA1448100 NM_001384479.1:c.1180_1182dup