Allele Registry

Canonical Allele Identifier: PA2826301586

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009195

RCV001762040

ClinVar Variation:

8663

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229391.1:p.His168Gln	CA119819 NM_001242462.1:c.504T>G CA359695513 NM_001242462.1:c.504T>A