Allele Registry

Canonical Allele Identifier: PA2830430592

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000756901

RCV001855883

RCV002332535

ClinVar Variation:

618484

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Arg120Gly	CA16621941 NM_198156.3:c.358C>G