Allele Registry

Canonical Allele Identifier: PA170679

Gene: P2RX2 HGNC NCBI

ClinVar RCV:

RCV000143842

ClinVar Variation:

155762

HGVS (amino-acid)	Matching Registered Transcripts
NP_036358.2:p.Arg37Leu	CA170678 NM_012226.5:c.110G>T