Canonical Allele Identifier: PA2828932769
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 1405037
ClinVar RCV Id: RCV001927889 RCV002507013
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369746.2:p.Asp318His
CA1448172
NM_001382817.3:c.952G>C