Allele Registry

Canonical Allele Identifier: PA108421

Gene: VHL HGNC NCBI

ClinVar Allele:

224955

ClinVar RCV:

RCV000208789

RCV003278699

ClinVar Variation:

223225

HGVS (amino-acid)	Matching Registered Transcripts
NP_000542.1:p.Cys162Tyr	CA357010 NM_000551.4:c.485G>A