Canonical Allele Identifier: PA203555
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 198686
ClinVar RCV Id: RCV000180093 RCV000186256 RCV000966394 RCV003937630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ile279Thr
CA203554
NM_000030.3:c.836T>C