Canonical Allele Identifier: PA645434235
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 353681
ClinVar RCV Id: RCV000380451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000154.1:p.Leu220Phe
CA3254467
NM_000163.5:c.660G>T
CA359695866
NM_000163.5:c.660G>C