Canonical Allele Identifier: PA2826299877
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 8637
ClinVar RCV Id: RCV000009169 RCV000723957 RCV000660368 RCV000764609 RCV001156022 RCV003478972 RCV003398475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229332.1:p.Arg179Cys
CA119799
NM_001242403.3:c.535C>T