Allele Registry

Canonical Allele Identifier: PA2573159772

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV002019332

ClinVar Variation:

1497047

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly47Trp	CA351313239 NM_000030.3:c.139G>T