Allele Registry

Canonical Allele Identifier: PA091328

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000169358

RCV001386996

ClinVar Variation:

188979

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ser218Leu	CA274210 NM_000030.3:c.653C>T