Canonical Allele Identifier: PA2825163318
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1944966
ClinVar RCV Id: RCV002640042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Met95Ile
CA357055398
NM_000406.3:c.285G>T
CA357055399
NM_000406.3:c.285G>C
CA357055400
NM_000406.3:c.285G>A