Canonical Allele Identifier: PA275740
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204128
ClinVar RCV Id: RCV000186334 RCV001852425 RCV002282021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Leu269Pro
CA275739
NM_000030.3:c.806T>C