Allele Registry

Canonical Allele Identifier: PA916057415

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000030583

RCV000486047

RCV000492682

RCV000816283

ClinVar Variation:

36900

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Arg107Pro	CA020262 NM_198156.3:c.320G>C CA645524845 NM_198156.3:c.320_321delinsCA