Allele Registry

Canonical Allele Identifier: PA108592

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000002323

RCV001219111

ClinVar Variation:

2235

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.His191Asp	CA020495 NM_000551.4:c.571C>G