Canonical Allele Identifier: PA2580240480
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 2063617
ClinVar RCV Id: RCV002948598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371408.1:p.Gly255Ser
CA1448231
NM_001384479.1:c.763G>A