Allele Registry

Canonical Allele Identifier: PA645463322

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000481472

RCV000631259

RCV000764460

RCV001024946

ClinVar Variation:

421823

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Arg205His	CA041951 NM_000551.4:c.614G>A