Allele Registry

Canonical Allele Identifier: PA091307

Gene: AGXT HGNC NCBI

ClinVar Allele:

200505

ClinVar RCV:

RCV000186314

ClinVar Variation:

204108

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Cys173Tyr	CA275703 NM_000030.3:c.518G>A