Allele Registry

Canonical Allele Identifier: PA269997

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000128827

ClinVar Variation:

140611

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Thr269Met	CA269995 NM_000406.3:c.806C>T