Allele Registry

Canonical Allele Identifier: PA2580279367

Gene: P2RY11 HGNC NCBI

ClinVar RCV:

RCV004258355

ClinVar Variation:

2465258

HGVS (amino-acid)	Matching Registered Transcripts
NP_002557.2:p.Pro84Ser	CA9186354 NM_002566.5:c.250C>T