Allele Registry

Canonical Allele Identifier: PA185872

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000156945

RCV000995775

ClinVar Variation:

180147

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Leu117Arg	CA185871 NM_000406.3:c.350T>G