Allele Registry

Canonical Allele Identifier: PA913197371

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000767232

RCV001037923

ClinVar Variation:

625220

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Leu63Gln	CA351748753 NM_000551.4:c.188T>A