Allele Registry

Canonical Allele Identifier: PA2827926889

Gene: VHL HGNC NCBI

ClinVar Allele:

2794811

ClinVar RCV:

RCV003388486

ClinVar Variation:

2627292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Tyr98Asn	CA351750883 NM_001354723.2:c.292T>A