Allele Registry

Canonical Allele Identifier: PA275738

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186333

ClinVar Variation:

204127

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.His261Gln	CA275737 NM_000030.3:c.783T>A CA351318300 NM_000030.3:c.783T>G