Canonical Allele Identifier: PA2825075734
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2847517
ClinVar RCV Id: RCV003692809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000154.1:p.Val147Ala
CA359695383
NM_000163.5:c.440T>C