Allele Registry

Canonical Allele Identifier: PA2741809227

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV003468677

ClinVar Variation:

2681152

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Val8Asp	CA2586971624 NM_000030.3:c.23_24delinsAT