Canonical Allele Identifier: PA2828932759
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 2063617
ClinVar RCV Id: RCV002948598
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369746.2:p.Gly255Ser
CA1448231
NM_001382817.3:c.763G>A