Allele Registry

Canonical Allele Identifier: PA2827926637

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001233308

RCV002484277

ClinVar Variation:

959877

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Gly44Arg	CA351748058 NM_001354723.2:c.130G>C