Allele Registry

Canonical Allele Identifier: PA096638

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009186

RCV003322747

ClinVar Variation:

8654

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Ile171Thr	CA119812 NM_000163.5:c.512T>C