Allele Registry

Canonical Allele Identifier: PA658662437

Gene: PRX HGNC NCBI

ClinVar RCV:

RCV000554182

RCV001131934

RCV001546675

RCV002377182

ClinVar Variation:

476979

HGVS (amino-acid)	Matching Registered Transcripts
NP_870998.2:p.Arg240Gln	CA9444391 NM_181882.3:c.719G>A