Allele Registry

Canonical Allele Identifier: PA091326

Gene: AGXT HGNC NCBI

ClinVar Allele:

150265

ClinVar RCV:

RCV000128801

RCV003317095

ClinVar Variation:

140584

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ser187Phe	CA345702 NM_000030.3:c.560C>T