Canonical Allele Identifier: PA916005600
Gene: GHR HGNC NCBI
ClinVar Allele:
23675
ClinVar RCV:
RCV000009168
ClinVar Variation:
8636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229328.1:p.Glu69Lys
CA119798
NM_001242399.2:c.205G>A