Allele Registry

Canonical Allele Identifier: PA2826301291

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009180

ClinVar Variation:

8648

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Val151Gly	CA119807 NM_001242460.1:c.452T>G