Allele Registry

Canonical Allele Identifier: PA2826299877

Gene: GHR HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

23676

ClinVar RCV:

RCV000009169

RCV000660368

RCV000723957

RCV000764609

RCV001156022

RCV003398475

RCV003478972

ClinVar Variation:

8637

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229332.1:p.Arg179Cys	CA119799 NM_001242403.3:c.535C>T