Allele Registry

Canonical Allele Identifier: PA2826299298

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV001157738

RCV001859027

ClinVar Variation:

907708

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229330.1:p.Glu242Lys	CA3254478 NM_001242401.4:c.724G>A