Allele Registry

Canonical Allele Identifier: PA2825315382

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030911

ClinVar Variation:

16027

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012781.1:p.Leu175Met	CA130204 NM_001012763.2:c.523C>A