Canonical Allele Identifier: PA915956401
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 16032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012781.1:p.Glu90Lys
CA130209
NM_001012763.2:c.268G>A