Allele Registry

Canonical Allele Identifier: PA269462

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000114425

ClinVar Variation:

126541

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Thr32Ala	CA269461 NM_000406.3:c.94A>G