Canonical Allele Identifier: PA2580130916
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2009505
ClinVar RCV Id: RCV002838481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012781.1:p.Arg139Leu
CA357054555
NM_001012763.2:c.416G>T