Allele Registry

Canonical Allele Identifier: PA915956405

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000128826

ClinVar Variation:

140610

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012781.1:p.Met131Thr	CA269993 NM_001012763.2:c.392T>C