Canonical Allele Identifier: PA916005698
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 281095
ClinVar RCV Id: RCV000342816 RCV000392588 RCV001572964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229328.1:p.Cys447Phe
CA3254634
NM_001242399.2:c.1340G>T