Canonical Allele Identifier: PA2580130919
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1722804
ClinVar RCV Id: RCV002305911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012781.1:p.Val247Ala
CA357047648
NM_001012763.2:c.740T>C