Allele Registry

Canonical Allele Identifier: PA2827926839

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000417911

ClinVar Variation:

376047

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Leu89His	CA16602514 NM_001354723.2:c.266T>A