Allele Registry

Canonical Allele Identifier: PA3057504591

Gene: GHR HGNC NCBI

ClinVar Allele:

3743235

ClinVar RCV:

RCV005062243

ClinVar Variation:

3604484

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229391.1:p.Trp4Arg	CA3254278 NM_001242462.1:c.10T>C CA359694394 NM_001242462.1:c.10T>A