Canonical Allele Identifier: PA913198216
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 632446
ClinVar RCV Id: RCV000779451 RCV003546600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Val94Ala
CA2938965
NM_000406.3:c.281T>C