Canonical Allele Identifier: PA915956398
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 493395
ClinVar RCV Id: RCV000585491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012781.1:p.Leu48Pro
CA357056271
NM_001012763.2:c.143T>C