Canonical Allele Identifier: PA2828967219
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 3097223
ClinVar RCV Id: RCV004387057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371408.1:p.His209Tyr
CA345206101
NM_001384479.1:c.625C>T