Allele Registry

Canonical Allele Identifier: PA2826301325

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV001157738

RCV001859027

ClinVar Variation:

907708

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Glu220Lys	CA3254478 NM_001242460.1:c.658G>A