Allele Registry

Canonical Allele Identifier: PA2827926717

Gene: VHL HGNC NCBI

ClinVar Allele:

139664

ClinVar RCV:

RCV000123103

RCV001588972

ClinVar Variation:

135952

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Arg64His	CA020083 NM_001354723.2:c.191G>A