Canonical Allele Identifier: PA2580111194
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2079685
ClinVar RCV Id: RCV002998711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Trp280Cys
CA357047836
NM_000406.3:c.840G>T
CA357047839
NM_000406.3:c.840G>C