Allele Registry

Canonical Allele Identifier: PA275680

Gene: AGXT HGNC NCBI

ClinVar Allele:

200476

ClinVar RCV:

RCV000186302

ClinVar Variation:

204096

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Arg118His	CA275679 NM_000030.3:c.353G>A