Canonical Allele Identifier: PA915956412
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 717649
ClinVar RCV Id: RCV000890475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012781.1:p.Thr219Ala
CA357048339
NM_001012763.2:c.655A>G