Allele Registry

Canonical Allele Identifier: PA275714

Gene: AGXT HGNC NCBI

ClinVar Allele:

200518

ClinVar RCV:

RCV000186320

ClinVar Variation:

204114

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly199Ser	CA275713 NM_000030.3:c.595G>A