Allele Registry

Canonical Allele Identifier: PA2499302231

Gene: PRX HGNC NCBI

ClinVar RCV:

RCV001366553

ClinVar Variation:

1057546

HGVS (amino-acid)	Matching Registered Transcripts
NP_870998.2:p.Arg196Gly	CA405900098 NM_181882.3:c.586C>G