Allele Registry

Canonical Allele Identifier: PA275639

Gene: AGXT HGNC NCBI

ClinVar Allele:

200448

ClinVar RCV:

RCV000186283

RCV003229816

RCV003230441

ClinVar Variation:

204077

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ile56Asn	CA275638 NM_000030.3:c.167T>A