Canonical Allele Identifier: PA916005749
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 492772
ClinVar RCV Id: RCV000582223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229391.1:p.Trp4Cys
CA359694400
NM_001242462.1:c.12G>C
CA359694401
NM_001242462.1:c.12G>T