Allele Registry

Canonical Allele Identifier: PA2826301300

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000240723

ClinVar Variation:

254180

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Trp165Arg	CA10586364 NM_001242460.1:c.493T>C CA359695629 NM_001242460.1:c.493T>A