Allele Registry

Canonical Allele Identifier: PA2826299259

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009185

RCV002508773

ClinVar Variation:

8653

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229330.1:p.Asp170His	CA119811 NM_001242401.4:c.508G>C