Allele Registry

Canonical Allele Identifier: PA1139693040

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV001157738

RCV001859027

ClinVar Variation:

907708

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.Glu249Lys	CA3254478 NM_001242399.2:c.745G>A