Allele Registry

Canonical Allele Identifier: PA2825191230

Gene: VHL HGNC NCBI

ClinVar Allele:

2794811

ClinVar RCV:

RCV003388486

ClinVar Variation:

2627292

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Tyr98Asn	CA351750883 NM_000551.4:c.292T>A