Canonical Allele Identifier: PA2826299822
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 353679
ClinVar RCV Id: RCV000377004 RCV000872811 RCV003155171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229332.1:p.Thr69Ile
CA3254351
NM_001242403.3:c.206C>T