Canonical Allele Identifier: PA2580130912
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2225908
ClinVar RCV Id: RCV002727399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012781.1:p.Trp63Arg
CA357056085
NM_001012763.2:c.187T>C
CA357056086
NM_001012763.2:c.187T>A