Canonical Allele Identifier: PA091324
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 5645
ClinVar RCV Id: RCV000005999 RCV000727639 RCV000779687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Phe152Ile
CA340444
NM_000030.3:c.454T>A