Allele Registry

Canonical Allele Identifier: PA200656

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009190

RCV000173652

RCV000392579

RCV001701562

RCV001719693

ClinVar Variation:

8658

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Ile544Leu	CA200655 NM_000163.5:c.1630A>C