Allele Registry

Canonical Allele Identifier: PA108827

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002315

RCV000585971

RCV000704785

ClinVar Variation:

2227

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Leu63Pro	CA020079 NM_000551.4:c.188T>C