Allele Registry

Canonical Allele Identifier: PA275708

Gene: AGXT HGNC NCBI

ClinVar Allele:

200510

ClinVar RCV:

RCV000186316

RCV002513968

ClinVar Variation:

204110

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Cys178Tyr	CA275707 NM_000030.3:c.533G>A