Allele Registry

Canonical Allele Identifier: PA2827926837

Gene: VHL HGNC NCBI

ClinVar Allele:

17259

ClinVar RCV:

RCV000002306

ClinVar Variation:

2220

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Trp88Ser	CA020202 NM_001354723.2:c.263G>C