Canonical Allele Identifier: PA2741809312
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2681181
ClinVar RCV Id: RCV003468706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Leu211Arg
CA351316895
NM_000030.3:c.632T>G