Canonical Allele Identifier: PA2826299232
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 492773
ClinVar RCV Id: RCV000581563 RCV002469211
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229330.1:p.Trp122Arg
CA359695204
NM_001242401.4:c.364T>A
CA359695205
NM_001242401.4:c.364T>C