Canonical Allele Identifier: PA2825163294
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 904872
ClinVar RCV Id: RCV001153045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Ser4Arg
CA2939016
NM_000406.3:c.12T>G
CA357056909
NM_000406.3:c.12T>A
CA357056924
NM_000406.3:c.10A>C