Allele Registry

Canonical Allele Identifier: PA2825075747

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV001727321

ClinVar Variation:

1298991

HGVS (amino-acid)	Matching Registered Transcripts
NP_000154.1:p.His168Pro	CA3254422 NM_000163.5:c.503A>C