Allele Registry

Canonical Allele Identifier: PA287851

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000115746

RCV000208783

RCV000492260

RCV001854559

ClinVar Variation:

127829

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Ala149Ser	CA020355 NM_000551.4:c.445G>T