Allele Registry

Canonical Allele Identifier: PA916005743

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009194

ClinVar Variation:

8662

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Cys90Ser	CA119817 NM_001242460.1:c.269G>C CA359695137 NM_001242460.1:c.268T>A