Canonical Allele Identifier: PA658662200
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 449369
ClinVar RCV Id: RCV000522157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000154.1:p.Gly80Val
CA3254355
NM_000163.5:c.239G>T