Canonical Allele Identifier: PA2826300466
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2847517
ClinVar RCV Id: RCV003692809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229334.1:p.Val147Ala
CA359695383
NM_001242405.2:c.440T>C