Allele Registry

Canonical Allele Identifier: PA2827926860

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000208845

ClinVar Variation:

223175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Gly93Cys	CA357106 NM_001354723.2:c.277G>T