Allele Registry

Canonical Allele Identifier: PA108199

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000756901

RCV001855883

RCV002332535

ClinVar Variation:

618484

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Arg161Gly	CA16621941 NM_000551.4:c.481C>G