Allele Registry

Canonical Allele Identifier: PA108336

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000079207

RCV000254892

RCV000492165

RCV001034687

ClinVar Variation:

93326

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Asn78Ser	CA020131 NM_000551.4:c.233A>G