Allele Registry

Canonical Allele Identifier: PA2826298949

Gene: GHR HGNC NCBI

ClinVar Allele:

227287

ClinVar RCV:

RCV000490420

ClinVar Variation:

225374

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229329.1:p.Gly166Glu	CA3254420 NM_001242400.2:c.497G>A