Canonical Allele Identifier: PA2826300785
Gene: GHR HGNC NCBI
ClinVar Allele:
227287
ClinVar RCV:
RCV000490420
ClinVar Variation:
225374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229335.1:p.Gly166Glu
CA3254420
NM_001242406.2:c.497G>A