Allele Registry

Canonical Allele Identifier: PA645434192

Gene: GHR HGNC NCBI

ClinVar Allele:

227287

ClinVar RCV:

RCV000490420

ClinVar Variation:

225374

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Gly166Glu	CA3254420 NM_000163.5:c.497G>A