Allele Registry

Canonical Allele Identifier: PA108556

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002325

RCV000208813

RCV000698471

RCV002433441

RCV003460405

ClinVar Variation:

2237

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Gly93Ser	CA020230 NM_000551.4:c.277G>A