Allele Registry

Canonical Allele Identifier: PA108975

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000079208

RCV000723702

RCV001227827

ClinVar Variation:

93327

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Pro86Ala	CA020174 NM_000551.4:c.256C>G