Allele Registry

Canonical Allele Identifier: PA096628

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009168

ClinVar Variation:

8636

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Glu62Lys	CA119798 NM_000163.5:c.184G>A