Allele Registry

Canonical Allele Identifier: PA2825190721

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000823930

RCV002381882

ClinVar Variation:

665608

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Pro45Ala	CA351748071 NM_000551.4:c.133C>G