Canonical Allele Identifier: PA658825417
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 548671
ClinVar RCV Id: RCV000662314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Arg360Pro
CA351319729
NM_000030.3:c.1079G>C