Allele Registry

Canonical Allele Identifier: PA275782

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186353

ClinVar Variation:

204146

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Leu359Pro	CA275781 NM_000030.3:c.1076T>C