Allele Registry

Canonical Allele Identifier: PA2826301280

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV001946003

RCV002491956

ClinVar Variation:

1427764

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229389.1:p.Val140Phe	CA3254418 NM_001242460.1:c.418G>T