Canonical Allele Identifier: PA2825163315
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 3100699
ClinVar RCV Id: RCV004395576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Arg75Ser
CA2938969
NM_000406.3:c.225A>C
CA357055824
NM_000406.3:c.225A>T