Canonical Allele Identifier: PA2825163363
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 349452
ClinVar RCV Id: RCV000404324
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Ile258Thr
CA10621558
NM_000406.3:c.773T>C