Allele Registry

Canonical Allele Identifier: PA916005746

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009164

ClinVar Variation:

8632

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Phe92Ser	CA119790 NM_001242460.1:c.275T>C