Allele Registry

Canonical Allele Identifier: PA275722

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186324

RCV001857589

RCV002307437

ClinVar Variation:

204118

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ser205Leu	CA275721 NM_000030.3:c.614C>T