Canonical Allele Identifier: PA2580102547
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2203299
ClinVar RCV Id: RCV002651634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Arg360Trp
CA2209414
NM_000030.3:c.1078C>T