Allele Registry

Canonical Allele Identifier: PA091304

Gene: AGXT HGNC NCBI

ClinVar Allele:

200511

ClinVar RCV:

RCV000186317

ClinVar Variation:

204111

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Asp183Asn	CA275709 NM_000030.3:c.547G>A