Allele Registry

Canonical Allele Identifier: PA916057147

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002314

RCV000132356

RCV000208872

RCV000475973

RCV000679019

ClinVar Variation:

2226

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Arg64Pro	CA020089 NM_198156.3:c.191G>C