Canonical Allele Identifier: PA2826300207
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 281656
ClinVar RCV Id: RCV000292438 RCV000660599 RCV000724936 RCV001156023
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229333.1:p.Arg229His
CA3254474
NM_001242404.2:c.686G>A