Allele Registry

Canonical Allele Identifier: PA108875

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000589290

RCV000767268

ClinVar Variation:

496065

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Phe136Cys	CA70049495 NM_000551.4:c.407T>G