Allele Registry

Canonical Allele Identifier: PA2830430889

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000148924

RCV000589801

RCV000698671

RCV001024290

RCV003467207

ClinVar Variation:

161403

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Glu145Lys	CA020480 NM_198156.3:c.433G>A