Allele Registry

Canonical Allele Identifier: PA275660

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186293

RCV001352204

ClinVar Variation:

204087

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Glu95Lys	CA275659 NM_000030.3:c.283G>A