Canonical Allele Identifier: PA2825163325
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2171057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000397.1:p.Ala127Val
CA2938952
NM_000406.3:c.380C>T