Allele Registry

Canonical Allele Identifier: PA2827926811

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000173161

RCV000724457

ClinVar Variation:

193118

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Arg82Pro	CA020159 NM_001354723.2:c.245G>C