Canonical Allele Identifier: PA2826299587
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1186321
ClinVar RCV Id: RCV001545379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229331.1:p.Tyr218Cys
CA3254465
NM_001242402.2:c.653A>G