Allele Registry

Canonical Allele Identifier: PA275717

Gene: AGXT HGNC NCBI

ClinVar Allele:

200521

ClinVar RCV:

RCV000186322

ClinVar Variation:

204116

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ile202Asn	CA275716 NM_000030.3:c.605T>A