Allele Registry

Canonical Allele Identifier: PA108795

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002311

RCV000002312

RCV000002313

RCV000210199

RCV000480890

RCV000627743

RCV003330076

ClinVar Variation:

2225

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Leu188Val	CA020488 NM_000551.4:c.562C>G