Allele Registry

Canonical Allele Identifier: PA916005635

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009180

ClinVar Variation:

8648

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.Val180Gly	CA119807 NM_001242399.2:c.539T>G