Allele Registry

Canonical Allele Identifier: PA645392954

Gene: GHRHR HGNC NCBI

ClinVar RCV:

RCV000489482

ClinVar Variation:

427035

HGVS (amino-acid)	Matching Registered Transcripts
NP_000814.2:p.Pro336Leu	CA4208758 NM_000823.4:c.1007C>T