Canonical Allele Identifier: PA2826299281
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1186321
ClinVar RCV Id: RCV001545379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229330.1:p.Tyr218Cys
CA3254465
NM_001242401.4:c.653A>G