Allele Registry

Canonical Allele Identifier: PA275786

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186355

ClinVar Variation:

204148

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ala368Thr	CA275785 NM_000030.3:c.1102G>A