Allele Registry

Canonical Allele Identifier: PA916057305

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000417911

ClinVar Variation:

376047

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Leu89His	CA16602514 NM_198156.3:c.266T>A