Canonical Allele Identifier: PA2826300813
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 3068226
ClinVar RCV Id: RCV003991906
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229335.1:p.Ser219Pro
CA359695857
NM_001242406.2:c.655T>C