Allele Registry

Canonical Allele Identifier: PA275567

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186235

ClinVar Variation:

204031

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ser99Tyr	CA275566 NM_000030.3:c.296C>A