Allele Registry

Canonical Allele Identifier: PA2825785804

Gene: GHRL HGNC NCBI

ClinVar RCV:

RCV004390569

ClinVar Variation:

3099744

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128416.1:p.Ala56Ser	CA2252365 NM_001134944.2:c.166G>T