Allele Registry

Canonical Allele Identifier: PA2826299839

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009164

ClinVar Variation:

8632

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229332.1:p.Phe114Ser	CA119790 NM_001242403.3:c.341T>C