Allele Registry

Canonical Allele Identifier: PA104883

Gene: GNRHR HGNC NCBI

ClinVar RCV:

RCV000030911

ClinVar Variation:

16027

HGVS (amino-acid)	Matching Registered Transcripts
NP_000397.1:p.Ser217Arg	CA130204 NM_000406.3:c.651C>A CA357050709 NM_000406.3:c.651C>G CA357050718 NM_000406.3:c.649A>C