Allele Registry

Canonical Allele Identifier: PA119818

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009194

ClinVar Variation:

8662

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Cys112Ser	CA119817 NM_000163.5:c.335G>C CA359695137 NM_000163.5:c.334T>A