Allele Registry

Canonical Allele Identifier: PA117239

Gene: GHRL HGNC NCBI

ClinVar RCV:

RCV000005364

RCV000033194

ClinVar Variation:

5061

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128416.1:p.Arg39Gln	CA117238 NM_001134944.2:c.116G>A