Canonical Allele Identifier: PA645434192
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 225374
ClinVar RCV Id: RCV000490420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000154.1:p.Gly166Glu
CA3254420
NM_000163.5:c.497G>A