Canonical Allele Identifier: PA2580240470
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 2135150
ClinVar RCV Id: RCV003048490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371408.1:p.Ser68Cys
CA345207403
NM_001384479.1:c.203C>G