Allele Registry

Canonical Allele Identifier: PA2741809258

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV003319773

ClinVar Variation:

2574876

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly97Arg	CA351313733 NM_000030.3:c.289G>C CA351313736 NM_000030.3:c.289G>A