Allele Registry

Canonical Allele Identifier: PA2826874357

Gene: GHRL HGNC NCBI

ClinVar RCV:

RCV000023422

RCV001723541

ClinVar Variation:

5063

HGVS (amino-acid)	Matching Registered Transcripts
NP_001289752.1:p.Gln89Leu	CA210809 NM_001302823.2:c.266A>T