Allele Registry

Canonical Allele Identifier: PA2826298750

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009164

ClinVar Variation:

8632

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.Phe121Ser	CA119790 NM_001242399.2:c.362T>C