Allele Registry

Canonical Allele Identifier: PA275780

Gene: AGXT HGNC NCBI

ClinVar Allele:

200597

ClinVar RCV:

RCV000186352

ClinVar Variation:

204145

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly349Ser	CA275779 NM_000030.3:c.1045G>A