Canonical Allele Identifier: PA2826300734
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 8636
ClinVar RCV Id: RCV000009168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229335.1:p.Glu62Lys
CA119798
NM_001242406.2:c.184G>A