Allele Registry

Canonical Allele Identifier: PA104832

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030916

RCV001560549

ClinVar Variation:

16032

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Glu90Lys	CA130209 NM_000406.3:c.268G>A