Allele Registry

Canonical Allele Identifier: PA916005645

Gene: GHR HGNC NCBI

ClinVar RCV:

RCV000240723

ClinVar Variation:

254180

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229328.1:p.Trp194Arg	CA10586364 NM_001242399.2:c.580T>C CA359695629 NM_001242399.2:c.580T>A