Canonical Allele Identifier: PA2825163375
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1709893
ClinVar RCV Id: RCV002290235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Pro282Leu
CA357047799
NM_000406.3:c.845C>T