Allele Registry

Canonical Allele Identifier: PA2826301286

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV001727321

ClinVar Variation:

1298991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.His146Pro	CA3254422 NM_001242460.1:c.437A>C