Canonical Allele Identifier: PA2580240475
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 2060541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371408.1:p.Val124Ile
CA1448312
NM_001384479.1:c.370G>A