Allele Registry

Canonical Allele Identifier: PA091312

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000032681

RCV000432954

RCV000589490

RCV003407388

RCV003552420

ClinVar Variation:

40166

2710435

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly170Arg	CA343785 NM_000030.3:c.508G>A CA68178405 NM_000030.3:c.508G>C