Canonical Allele Identifier: PA2825163336
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1304993
ClinVar RCV Id: RCV001765168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Thr144Pro
CA357054516
NM_000406.3:c.430A>C