Allele Registry

Canonical Allele Identifier: PA2826301273

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009183

ClinVar Variation:

8651

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Pro127Gln	CA119808 NM_001242460.1:c.380C>A