Allele Registry

Canonical Allele Identifier: PA275637

Gene: AGXT HGNC NCBI

ClinVar Allele:

200437

2842240

ClinVar RCV:

RCV000186282

RCV001067805

RCV003468719

ClinVar Variation:

204076

2681194

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly47Arg	CA275636 NM_000030.3:c.139G>A CA2208986 NM_000030.3:c.139G>C