Allele Registry

Canonical Allele Identifier: PA645374537

Gene: PRX HGNC NCBI

ClinVar RCV:

RCV000235608

RCV000658835

RCV001085498

RCV001128999

RCV001172782

RCV001358805

RCV002450720

ClinVar Variation:

245663

HGVS (amino-acid)	Matching Registered Transcripts
NP_870998.2:p.Gly1125Ser	CA9443872 NM_181882.3:c.3373G>A