Canonical Allele Identifier: PA2826298869
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 492772
ClinVar RCV Id: RCV000582223
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229329.1:p.Trp4Cys
CA359694400
NM_001242400.2:c.12G>C
CA359694401
NM_001242400.2:c.12G>T