Allele Registry

Canonical Allele Identifier: PA108549

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000208845

ClinVar Variation:

223175

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Gly93Cys	CA357106 NM_000551.4:c.277G>T