Canonical Allele Identifier: PA2826300490
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 8637
ClinVar RCV Id: RCV000009169 RCV000723957 RCV000660368 RCV000764609 RCV001156022 RCV003478972 RCV003398475
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229334.1:p.Arg179Cys
CA119799
NM_001242405.2:c.535C>T