Allele Registry

Canonical Allele Identifier: PA130215

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030920

ClinVar Variation:

16036

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Pro320Leu	CA130214 NM_000406.3:c.959C>T