Allele Registry

Canonical Allele Identifier: PA096617

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009177

ClinVar Variation:

8645

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.Gln172Pro	CA119804 NM_000163.5:c.515A>C