Canonical Allele Identifier: PA170679
Gene: P2RX2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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