Allele Registry

Canonical Allele Identifier: PA1139668739

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV001235996

RCV001828877

ClinVar Variation:

962187

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Pro96Ala	CA351313721 NM_000030.3:c.286C>G