Allele Registry

Canonical Allele Identifier: PA2741809259

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV003445266

ClinVar Variation:

2664120

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Asp98His	CA351313747 NM_000030.3:c.292G>C