Allele Registry

Canonical Allele Identifier: PA2580130914

Gene: GNRHR HGNC NCBI

ClinVar Variation Id: 1944966

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012781.1:p.Met95Ile	CA357055398 NM_001012763.2:c.285G>T CA357055399 NM_001012763.2:c.285G>C CA357055400 NM_001012763.2:c.285G>A