Canonical Allele Identifier: PA2741992995
Gene: AGXT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2533948
ClinVar RCV Id: RCV004308495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114106.1:p.Ala484Val
CA3228928
NM_031900.4:c.1451C>T