Canonical Allele Identifier: PA275632
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204074
ClinVar RCV Id: RCV000186280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly42Glu
CA275631
NM_000030.3:c.125G>A