Allele Registry

Canonical Allele Identifier: PA119820

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009195

RCV001762040

ClinVar Variation:

8663

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.His168Gln	CA119819 NM_000163.5:c.504T>G CA359695513 NM_000163.5:c.504T>A