Allele Registry

Canonical Allele Identifier: PA109336

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002324

RCV000216720

RCV000588802

RCV001382229

RCV001851579

RCV002433440

RCV003884333

ClinVar Variation:

2236

229860

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Val84Leu	CA020170 NM_000551.4:c.250G>T CA10578180 NM_000551.4:c.250G>C