Allele Registry

Canonical Allele Identifier: PA104873

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030912

RCV001849269

ClinVar Variation:

16028

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Ser168Arg	CA130205 NM_000406.3:c.504T>A CA357054310 NM_000406.3:c.504T>G CA357054316 NM_000406.3:c.502A>C