Canonical Allele Identifier: PA916005628
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 8653
ClinVar RCV Id: RCV000009185 RCV002508773
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229328.1:p.Asp177His
CA119811
NM_001242399.2:c.529G>C