Allele Registry

Canonical Allele Identifier: PA916005630

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009186

RCV003322747

ClinVar Variation:

8654

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.Ile178Thr	CA119812 NM_001242399.2:c.533T>C