Allele Registry

Canonical Allele Identifier: PA658807396

Gene: PRX HGNC NCBI

ClinVar Allele:

532997

ClinVar RCV:

RCV000654259

RCV001811430

RCV002358894

RCV003945683

ClinVar Variation:

543486

HGVS (amino-acid)	Matching Registered Transcripts
NP_870998.2:p.Glu1280Gln	CA9443770 NM_181882.3:c.3838G>C