Canonical Allele Identifier: PA091314
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 188986
ClinVar RCV Id: RCV000169365 RCV001067841 RCV001328117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly350Asp
CA274217
NM_000030.3:c.1049G>A