Canonical Allele Identifier: PA2828932738
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 1601973
ClinVar RCV Id: RCV002127639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369746.2:p.Met96Val
CA1448331
NM_001382817.3:c.286A>G