Allele Registry

Canonical Allele Identifier: PA2826991356

Gene: GPR139 HGNC NCBI

ClinVar RCV:

RCV004173179

ClinVar Variation:

2334416

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305412.1:p.Ile112Val	CA7938306 NM_001318483.1:c.334A>G