Allele Registry

Canonical Allele Identifier: PA275766

Gene: AGXT HGNC NCBI

ClinVar Allele:

200587

ClinVar RCV:

RCV000186346

ClinVar Variation:

204139

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Leu316Pro	CA275765 NM_000030.3:c.947T>C