Allele Registry

Canonical Allele Identifier: PA2826301242

Gene: GHR HGNC NCBI

ClinVar Allele:

23675

ClinVar RCV:

RCV000009168

ClinVar Variation:

8636

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Glu40Lys	CA119798 NM_001242460.1:c.118G>A