Allele Registry

Canonical Allele Identifier: PA2826299564

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV001727321

ClinVar Variation:

1298991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229331.1:p.His168Pro	CA3254422 NM_001242402.2:c.503A>C