Canonical Allele Identifier: PA2573159782
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 1515099
ClinVar RCV Id: RCV002048424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly190Val
CA351316581
NM_000030.3:c.569G>T