Allele Registry

Canonical Allele Identifier: PA2827926643

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000823930

RCV002381882

ClinVar Variation:

665608

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Pro45Ala	CA351748071 NM_001354723.2:c.133C>G