ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA104775
Gene: GNRHR
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
31069
ClinVar RCV:
RCV000030914
RCV000497820
ClinVar Variation:
16030
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000397.1:p.Arg139His
CA249862
NM_000406.3:c.416G>A