Allele Registry

Canonical Allele Identifier: PA2825190897

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV003300745

ClinVar Variation:

2561023

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Leu63Arg	CA351748749 NM_000551.4:c.188T>G