Canonical Allele Identifier: PA275614
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204065
ClinVar RCV Id: RCV000186271 RCV001061218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Met1Thr