Canonical Allele Identifier: PA275630
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204073
ClinVar RCV Id: RCV000186279
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Gly41Glu
CA275629
NM_000030.3:c.122G>A