Allele Registry

Canonical Allele Identifier: PA091322

Gene: AGXT HGNC NCBI

ClinVar Allele:

200579

ClinVar RCV:

RCV000186343

ClinVar Variation:

204136

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Leu298Pro	CA275758 NM_000030.3:c.893T>C