Allele Registry

Canonical Allele Identifier: PA356687

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000204248

RCV000568942

RCV000662950

RCV001582712

RCV002467673

RCV003468958

ClinVar Variation:

220627

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Arg210Trp	CA041992 NM_000551.4:c.628C>T