Allele Registry

Canonical Allele Identifier: PA915956396

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000318227

RCV003989525

ClinVar Variation:

349458

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012781.1:p.Gln11Lys	CA2939012 NM_001012763.2:c.31C>A