Allele Registry

Canonical Allele Identifier: PA658669270

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000566330

RCV001046833

RCV001420952

RCV003465279

ClinVar Variation:

486714

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Pro154Ser	CA351754405 NM_000551.4:c.460C>T