Allele Registry

Canonical Allele Identifier: PA130212

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030919

RCV000498552

ClinVar Variation:

189195

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Asn10_Gln11delinsLysLys	CA130211 NM_000406.3:c.30_31delinsAA