Allele Registry

Canonical Allele Identifier: PA2826301285

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009195

RCV001762040

ClinVar Variation:

8663

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.His146Gln	CA119819 NM_001242460.1:c.438T>G CA359695513 NM_001242460.1:c.438T>A