Allele Registry

Canonical Allele Identifier: PA096727

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009180

ClinVar Variation:

8648

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Val173Gly	CA119807 NM_000163.5:c.518T>G