Canonical Allele Identifier: PA2825163383
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1722804
ClinVar RCV Id: RCV002305911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Tyr290His
CA357047648
NM_000406.3:c.868T>C