Canonical Allele Identifier: PA2826298773
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 3068226
ClinVar RCV Id: RCV003991906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229328.1:p.Ser226Pro
CA359695857
NM_001242399.2:c.676T>C