Allele Registry

Canonical Allele Identifier: PA091324

Gene: AGXT HGNC NCBI

ClinVar Allele:

20684

ClinVar RCV:

RCV000005999

RCV000727639

RCV000779687

ClinVar Variation:

5645

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Phe152Ile	CA340444 NM_000030.3:c.454T>A