Allele Registry

Canonical Allele Identifier: PA275823

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186387

RCV003330552

ClinVar Variation:

204180

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Glu95dup	CA275821 NM_000030.3:c.283_285dup