Allele Registry

Canonical Allele Identifier: PA915956401

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030916

RCV001560549

ClinVar Variation:

16032

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012781.1:p.Glu90Lys	CA130209 NM_001012763.2:c.268G>A