Allele Registry

Canonical Allele Identifier: PA275630

Gene: AGXT HGNC NCBI

ClinVar Allele:

200433

ClinVar RCV:

RCV000186279

ClinVar Variation:

204073

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