Allele Registry

Canonical Allele Identifier: PA357030

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000208800

RCV001379374

RCV001701790

ClinVar Variation:

223199

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Arg120Gly	CA357028 NM_000551.4:c.358A>G