Allele Registry

Canonical Allele Identifier: PA2826299271

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000240723

ClinVar Variation:

254180

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229330.1:p.Trp187Arg	CA10586364 NM_001242401.4:c.559T>C CA359695629 NM_001242401.4:c.559T>A