Allele Registry

Canonical Allele Identifier: PA2826299568

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009177

ClinVar Variation:

8645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229331.1:p.Gln172Pro	CA119804 NM_001242402.2:c.515A>C