Canonical Allele Identifier: PA2825163373
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1301193
ClinVar RCV Id: RCV001733271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Cys279Tyr
CA2938848
NM_000406.3:c.836G>A