Allele Registry

Canonical Allele Identifier: PA2826298747

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009194

ClinVar Variation:

8662

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.Cys119Ser	CA119817 NM_001242399.2:c.356G>C CA359695137 NM_001242399.2:c.355T>A