Allele Registry

Canonical Allele Identifier: PA119801

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009170

RCV002512935

ClinVar Variation:

8638

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Glu242Asp	CA119800 NM_000163.5:c.726G>C CA359696010 NM_000163.5:c.726G>T