Allele Registry

Canonical Allele Identifier: PA916005679

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009176

ClinVar Variation:

8644

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.Arg299Thr	CA212902 NM_001242399.2:c.896G>C