Canonical Allele Identifier: PA091331
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 188891
ClinVar RCV Id: RCV000169249 RCV000812967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Trp108Arg
CA274089
NM_000030.3:c.322T>C
CA351313841
NM_000030.3:c.322T>A