Allele Registry

Canonical Allele Identifier: PA645374440

Gene: PRX HGNC NCBI

ClinVar Allele:

245136

ClinVar RCV:

RCV000236385

RCV000764202

RCV000802296

RCV001136189

RCV002401925

RCV003333056

ClinVar Variation:

246316

HGVS (amino-acid)	Matching Registered Transcripts
NP_870998.2:p.Arg516Trp	CA9444242 NM_181882.3:c.1546C>T