Allele Registry

Canonical Allele Identifier: PA2825785812

Gene: GHRL HGNC NCBI

ClinVar RCV:

RCV004390569

ClinVar Variation:

3099744

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128417.1:p.Ala55Ser	CA2252365 NM_001134945.2:c.163G>T