Allele Registry

Canonical Allele Identifier: PA2830431025

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000204248

RCV000568942

RCV000662950

RCV001582712

RCV002467673

RCV003468958

ClinVar Variation:

220627

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Arg169Trp	CA041992 NM_198156.3:c.505C>T