Allele Registry

Canonical Allele Identifier: PA645462659

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000236098

RCV001011022

RCV001081208

RCV003998847

ClinVar Variation:

238100

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Pro45Arg	CA039433 NM_000551.4:c.134C>G