Allele Registry

Canonical Allele Identifier: PA3057250183

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV004587755

ClinVar Variation:

3251349

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012781.1:p.Ala129Val	CA357054682 NM_001012763.2:c.386C>T