Allele Registry

Canonical Allele Identifier: PA091302

Gene: AGXT HGNC NCBI

ClinVar Allele:

200539

ClinVar RCV:

RCV000186329

RCV001857590

ClinVar Variation:

204123

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Arg233Leu	CA275732 NM_000030.3:c.698G>T