Allele Registry

Canonical Allele Identifier: PA275667

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186296

ClinVar Variation:

204090

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly109Val	CA275666 NM_000030.3:c.326G>T