Allele Registry

Canonical Allele Identifier: PA645374301

Gene: PRX HGNC NCBI

ClinVar Allele:

410607

ClinVar RCV:

RCV000543868

RCV001173761

RCV001721548

ClinVar Variation:

418427

HGVS (amino-acid)	Matching Registered Transcripts
NP_870998.2:p.Pro298Ser	CA9444362 NM_181882.3:c.892C>T