Canonical Allele Identifier: PA2828932761
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 2247886
ClinVar RCV Id: RCV002748577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369746.2:p.Ala261Gly
CA345205781
NM_001382817.3:c.782C>G