Allele Registry

Canonical Allele Identifier: PA108173

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000036542

RCV000763091

RCV002321506

ClinVar Variation:

43599

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Arg107Gly	CA020257 NM_000551.4:c.319C>G