Canonical Allele Identifier: PA1139684849
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 904871
ClinVar RCV Id: RCV001153043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012781.1:p.Lys72Arg
CA357055888
NM_001012763.2:c.215A>G