Allele Registry

Canonical Allele Identifier: PA104775

Gene: GNRHR HGNC NCBI

ClinVar Allele:

31069

ClinVar RCV:

RCV000030914

RCV000497820

ClinVar Variation:

16030

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Arg139His	CA249862 NM_000406.3:c.416G>A