Allele Registry

Canonical Allele Identifier: PA645374338

Gene: PRX HGNC NCBI

ClinVar RCV:

RCV000459879

RCV001810956

ClinVar Variation:

410600

HGVS (amino-acid)	Matching Registered Transcripts
NP_870998.2:p.Arg464Gln	CA9444272 NM_181882.3:c.1391G>A