Allele Registry

Canonical Allele Identifier: PA170838

Gene: PTPRQ HGNC NCBI

ClinVar RCV:

RCV000144416

ClinVar Variation:

156332

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138498.1:p.Arg239Gly	CA170837 NM_001145026.2:c.715A>G