Allele Registry

Canonical Allele Identifier: PA2499242338

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV001727321

ClinVar Variation:

1298991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.His175Pro	CA3254422 NM_001242399.2:c.524A>C