Canonical Allele Identifier: PA658663837
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 451443
ClinVar RCV Id: RCV000523692 RCV001834701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Ala226Thr
CA351317085
NM_000030.3:c.676G>A