Allele Registry

Canonical Allele Identifier: PA645445775

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000478033

ClinVar Variation:

418236

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Asp138Gly	CA16618053 NM_000406.3:c.413A>G