Allele Registry

Canonical Allele Identifier: PA275690

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186306

RCV000668762

ClinVar Variation:

204100

553340

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Glu141Asp	CA275689 NM_000030.3:c.423G>T CA351314700 NM_000030.3:c.423G>C