Allele Registry

Canonical Allele Identifier: PA2826299938

Gene: GHR HGNC NCBI

ClinVar Allele:

23683

ClinVar RCV:

RCV000009176

ClinVar Variation:

8644

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229332.1:p.Arg292Thr	CA212902 NM_001242403.3:c.875G>C