Canonical Allele Identifier: PA2826301587
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 8653
ClinVar RCV Id: RCV000009185 RCV002508773
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229391.1:p.Asp170His
CA119811
NM_001242462.1:c.508G>C