Canonical Allele Identifier: PA269997
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 140611
ClinVar RCV Id: RCV000128827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Thr269Met
CA269995
NM_000406.3:c.806C>T