Allele Registry

Canonical Allele Identifier: PA130199

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030908

RCV000494391

RCV001849268

RCV002287337

ClinVar Variation:

16024

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Arg262Gln	CA130198 NM_000406.3:c.785G>A