Allele Registry

Canonical Allele Identifier: PA2826301591

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009180

ClinVar Variation:

8648

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229391.1:p.Val173Gly	CA119807 NM_001242462.1:c.518T>G