Allele Registry

Canonical Allele Identifier: PA2827926779

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000208790

RCV000469401

RCV000679023

RCV002444839

RCV003389711

ClinVar Variation:

223166

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Phe76del	CA357012 NM_001354723.2:c.227_229del