Canonical Allele Identifier: PA2580240478
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 2091998
ClinVar RCV Id: RCV003008096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371408.1:p.Val171Ile
CA345206402
NM_001384479.1:c.511G>A