Allele Registry

Canonical Allele Identifier: PA3057565483

Gene: AGT HGNC NCBI

ClinVar RCV:

RCV005009925

ClinVar Variation:

3581048

HGVS (amino-acid)	Matching Registered Transcripts
NP_001371408.1:p.Gln276Leu	CA345205684 NM_001384479.1:c.827A>T