Allele Registry

Canonical Allele Identifier: PA916005642

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009169

RCV000660368

RCV000723957

RCV000764609

RCV001156022

RCV003398475

RCV003478972

ClinVar Variation:

8637

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.Arg186Cys	CA119799 NM_001242399.2:c.556C>T