Allele Registry

Canonical Allele Identifier: PA104808

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000190591

RCV000255385

RCV000599632

RCV000662016

RCV001327939

RCV003330392

RCV003415714

RCV004018637

ClinVar Variation:

16023

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Gln106Arg	CA130197 NM_000406.3:c.317A>G