Allele Registry

Canonical Allele Identifier: PA275643

Gene: AGXT HGNC NCBI

ClinVar Allele:

200450

ClinVar RCV:

RCV000186285

ClinVar Variation:

204079

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly63Arg	CA275642 NM_000030.3:c.187G>C