Allele Registry

Canonical Allele Identifier: PA915956403

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000156945

RCV000995775

ClinVar Variation:

180147

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012781.1:p.Leu117Arg	CA185871 NM_001012763.2:c.350T>G