Allele Registry

Canonical Allele Identifier: PA108261

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002320

RCV000122262

RCV000148922

RCV000161094

RCV000574264

RCV000627742

RCV000722031

RCV002247239

ClinVar Variation:

2232

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Arg200Trp	CA020510 NM_000551.4:c.598C>T