Canonical Allele Identifier: PA2825163361
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 3100701
ClinVar RCV Id: RCV004395578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Leu249Pro
CA357048564
NM_000406.3:c.746T>C