Allele Registry

Canonical Allele Identifier: PA091313

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000169439

RCV000816747

RCV003324165

ClinVar Variation:

189047

2577088

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly190Arg	CA274318 NM_000030.3:c.568G>A CA351316577 NM_000030.3:c.568G>C