Allele Registry

Canonical Allele Identifier: PA119810

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009184

RCV000711804

RCV000987521

ClinVar Variation:

8652

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Val162Ile	CA119809 NM_000163.5:c.484G>A