Allele Registry

Canonical Allele Identifier: PA2825075808

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009176

ClinVar Variation:

8644

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Arg292Thr	CA212902 NM_000163.5:c.875G>C