Allele Registry

Canonical Allele Identifier: PA2826874353

Gene: GHRL HGNC NCBI

ClinVar RCV:

RCV004390569

ClinVar Variation:

3099744

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289752.1:p.Ala67Ser	CA2252365 NM_001302823.2:c.199G>T