Canonical Allele Identifier: PA275637
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204076
ClinVar RCV Id: RCV000186282 RCV001067805
ClinVar Variation Id: 2681194
ClinVar RCV Id: RCV003468719
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly47Arg
CA275636
NM_000030.3:c.139G>A
CA2208986
NM_000030.3:c.139G>C