Canonical Allele Identifier: PA2826300161
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2847517
ClinVar RCV Id: RCV003692809
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229333.1:p.Val147Ala
CA359695383
NM_001242404.2:c.440T>C