Allele Registry

Canonical Allele Identifier: PA645462846

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000417911

ClinVar Variation:

376047

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Leu89His	CA16602514 NM_000551.4:c.266T>A