Allele Registry

Canonical Allele Identifier: PA104892

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030909

ClinVar Variation:

16025

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Tyr284Cys	CA130201 NM_000406.3:c.851A>G