Allele Registry

Canonical Allele Identifier: PA915956397

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000114425

ClinVar Variation:

126541

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012781.1:p.Thr32Ala	CA269461 NM_001012763.2:c.94A>G