Allele Registry

Canonical Allele Identifier: PA916005631

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009177

ClinVar Variation:

8645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.Gln179Pro	CA119804 NM_001242399.2:c.536A>C