Allele Registry

Canonical Allele Identifier: PA091321

Gene: AGXT HGNC NCBI

ClinVar Allele:

200497

ClinVar RCV:

RCV000186308

ClinVar Variation:

204102

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Leu153Val	CA275693 NM_000030.3:c.457T>G