Allele Registry

Canonical Allele Identifier: PA269994

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000128826

ClinVar Variation:

140610

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Met131Thr	CA269993 NM_000406.3:c.392T>C