Allele Registry

Canonical Allele Identifier: PA2830430976

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002320

RCV000122262

RCV000148922

RCV000161094

RCV000574264

RCV000627742

RCV000722031

RCV002247239

ClinVar Variation:

2232

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Arg159Trp	CA020510 NM_198156.3:c.475C>T