Canonical Allele Identifier: PA658666860
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 451078
ClinVar RCV Id: RCV000523656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Trp63Cys
CA2938976
NM_000406.3:c.189G>C
CA357056054
NM_000406.3:c.189G>T