Allele Registry

Canonical Allele Identifier: PA3057565496

Gene: AGT HGNC NCBI

ClinVar RCV:

RCV005009877

ClinVar Variation:

3580974

HGVS (amino-acid)	Matching Registered Transcripts
NP_001371408.1:p.Arg366Trp	CA1448143 NM_001384479.1:c.1096C>T