Allele Registry

Canonical Allele Identifier: PA109079

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000036539

RCV000497340

RCV001219547

RCV002415465

ClinVar Variation:

43597

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Ser65Trp	CA020099 NM_000551.4:c.194C>G