Allele Registry

Canonical Allele Identifier: PA096661

Gene: GHR HGNC NCBI

ClinVar Allele:

23690

ClinVar RCV:

RCV000009183

ClinVar Variation:

8651

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Pro149Gln	CA119808 NM_000163.5:c.446C>A