Allele Registry

Canonical Allele Identifier: PA3057504587

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV005121440

ClinVar Variation:

3644513

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Ile522Val	CA359630656 NM_001242460.1:c.1564A>G