Allele Registry

Canonical Allele Identifier: PA2827926631

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV002269204

ClinVar Variation:

1697920

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Ser43Tyr	CA70042349 NM_001354723.2:c.128C>A