Allele Registry

Canonical Allele Identifier: PA2826301290

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000009177

ClinVar Variation:

8645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Gln150Pro	CA119804 NM_001242460.1:c.449A>C