Allele Registry

Canonical Allele Identifier: PA2826301327

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009170

RCV002512935

ClinVar Variation:

8638

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Glu220Asp	CA119800 NM_001242460.1:c.660G>C CA359696010 NM_001242460.1:c.660G>T