Canonical Allele Identifier: PA2826298921
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 8632
ClinVar RCV Id: RCV000009164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229329.1:p.Phe114Ser
CA119790
NM_001242400.2:c.341T>C