Allele Registry

Canonical Allele Identifier: PA2827926715

Gene: VHL HGNC NCBI

ClinVar Allele:

2717182

ClinVar RCV:

RCV003300745

ClinVar Variation:

2561023

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Leu63Arg	CA351748749 NM_001354723.2:c.188T>G