Canonical Allele Identifier: PA2826300514
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 281656
ClinVar RCV Id: RCV000292438 RCV000660599 RCV000724936 RCV001156023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229334.1:p.Arg229His
CA3254474
NM_001242405.2:c.686G>A