Canonical Allele Identifier: PA091315
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 5644
ClinVar RCV Id: RCV000005998 RCV000662315 RCV001221086 RCV002509145
ClinVar Variation Id: 2203295
ClinVar RCV Id: RCV002664289 RCV003466000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly41Arg
CA340443
NM_000030.3:c.121G>A
CA351313171
NM_000030.3:c.121G>C