Canonical Allele Identifier: PA2825163310
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2225908
ClinVar RCV Id: RCV002727399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Trp63Arg
CA357056085
NM_000406.3:c.187T>C
CA357056086
NM_000406.3:c.187T>A