Canonical Allele Identifier: PA2826301560
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 492773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229391.1:p.Trp122Arg
CA359695204
NM_001242462.1:c.364T>A
CA359695205
NM_001242462.1:c.364T>C