Allele Registry

Canonical Allele Identifier: PA275727

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186326

ClinVar Variation:

204120

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ala210Pro	CA275726 NM_000030.3:c.628G>C