Canonical Allele Identifier: PA2826299209
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 353679
ClinVar RCV Id: RCV000377004 RCV000872811 RCV003155171
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229330.1:p.Thr69Ile
CA3254351
NM_001242401.4:c.206C>T