Canonical Allele Identifier: PA2826300762
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 492773
ClinVar RCV Id: RCV000581563 RCV002469211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229335.1:p.Trp122Arg
CA359695204
NM_001242406.2:c.364T>A
CA359695205
NM_001242406.2:c.364T>C