Allele Registry

Canonical Allele Identifier: PA916005622

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009183

ClinVar Variation:

8651

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.Pro156Gln	CA119808 NM_001242399.2:c.467C>A