Canonical Allele Identifier: PA2580111198
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2002400
ClinVar RCV Id: RCV002820378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Tyr283Ser
CA357047786
NM_000406.3:c.848A>C