Allele Registry

Canonical Allele Identifier: PA658662449

Gene: PRX HGNC NCBI

ClinVar RCV:

RCV000539162

RCV001136190

RCV001565702

RCV002384261

RCV003915651

ClinVar Variation:

476949

HGVS (amino-acid)	Matching Registered Transcripts
NP_870998.2:p.Glu457Lys	CA9444276 NM_181882.3:c.1369G>A