Canonical Allele Identifier: PA916005748
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 807419
ClinVar RCV Id: RCV000995550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229389.1:p.Asn93Thr
CA359695162
NM_001242460.1:c.278A>C