Allele Registry

Canonical Allele Identifier: PA2826299857

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009183

ClinVar Variation:

8651

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229332.1:p.Pro149Gln	CA119808 NM_001242403.3:c.446C>A