Allele Registry

Canonical Allele Identifier: PA091330

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186218

RCV000314232

RCV001510634

ClinVar Variation:

204016

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Thr9Asn	CA275540 NM_000030.3:c.26C>A