Canonical Allele Identifier: PA2825163369
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1519153
ClinVar RCV Id: RCV002024394 RCV003225761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Leu266Arg
CA2938853
NM_000406.3:c.797T>G