Allele Registry

Canonical Allele Identifier: PA108368

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002318

RCV001236092

ClinVar Variation:

2230

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Asp126Tyr	CA020319 NM_000551.4:c.376G>T