Canonical Allele Identifier: PA2580111202
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2269477
ClinVar RCV Id: RCV002826242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Val304Leu
CA357047450
NM_000406.3:c.910G>T
CA357047456
NM_000406.3:c.910G>C