Allele Registry

Canonical Allele Identifier: PA645463082

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000474133

ClinVar Variation:

411955

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Leu163Arg	CA16611277 NM_000551.4:c.488T>G