Canonical Allele Identifier: PA2826299586
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2869168
ClinVar RCV Id: RCV003705365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229331.1:p.Pro216Ala
CA359695839
NM_001242402.2:c.646C>G