Canonical Allele Identifier: PA2826301239
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 353678
ClinVar RCV Id: RCV000329469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229389.1:p.Arg39Gln
CA3254348
NM_001242460.1:c.116G>A