Allele Registry

Canonical Allele Identifier: PA108837

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000161087

RCV000208869

RCV000817709

ClinVar Variation:

182979

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Leu89Pro	CA020207 NM_000551.4:c.266T>C