Allele Registry

Canonical Allele Identifier: PA104766

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030918

ClinVar Variation:

16034

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Ala171Thr	CA130210 NM_000406.3:c.511G>A