Allele Registry

Canonical Allele Identifier: PA2826874327

Gene: GHRL HGNC NCBI

ClinVar RCV:

RCV004390569

ClinVar Variation:

3099744

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289750.1:p.Ala68Ser	CA2252365 NM_001302821.2:c.202G>T