Canonical Allele Identifier: PA2826300911
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 281095
ClinVar RCV Id: RCV000342816 RCV000392588 RCV001572964
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229335.1:p.Cys440Phe
CA3254634
NM_001242406.2:c.1319G>T