Canonical Allele Identifier: PA2573216560
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 1557050
ClinVar RCV Id: RCV002194678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371408.1:p.Val130Leu
CA1448305
NM_001384479.1:c.388G>C