Allele Registry

Canonical Allele Identifier: PA104790

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030915

RCV000375229

ClinVar Variation:

16031

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Asn10Lys	CA130208 NM_000406.3:c.30T>A CA357056832 NM_000406.3:c.30T>G