Canonical Allele Identifier: PA2580130918
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2151986
ClinVar RCV Id: RCV003061549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012781.1:p.Thr219Met
CA2938854
NM_001012763.2:c.656C>T