Canonical Allele Identifier: PA091317
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204084
ClinVar RCV Id: RCV000186290 RCV001852424
ClinVar Variation Id: 2681157
ClinVar RCV Id: RCV003468682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly82Arg
CA275654
NM_000030.3:c.244G>C
CA351313532
NM_000030.3:c.244G>A