Canonical Allele Identifier: PA2741981329
Gene: GPR88 HGNC NCBI

Linked Data

ClinVar Variation Id: 2877821
ClinVar RCV Id: RCV003715158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071332.2:p.Pro238Ser
CA28152860
NM_022049.3:c.712C>T