Allele Registry

Canonical Allele Identifier: PA2826301353

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009176

ClinVar Variation:

8644

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Arg270Thr	CA212902 NM_001242460.1:c.809G>C