Allele Registry

Canonical Allele Identifier: PA2580121413

Gene: GPR139 HGNC NCBI

ClinVar RCV:

RCV004173179

ClinVar Variation:

2334416

HGVS (amino-acid)	Matching Registered Transcripts
NP_001002911.1:p.Ile205Val	CA7938306 NM_001002911.4:c.613A>G