Allele Registry

Canonical Allele Identifier: PA109171

Gene: VHL HGNC NCBI

ClinVar Allele:

17267

ClinVar RCV:

RCV000002316

ClinVar Variation:

2228

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Tyr112Asn	CA020273 NM_000551.4:c.334T>A