Allele Registry

Canonical Allele Identifier: PA2830430601

Gene: VHL HGNC NCBI

ClinVar Allele:

224955

ClinVar RCV:

RCV000208789

RCV003278699

ClinVar Variation:

223225

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Cys121Tyr	CA357010 NM_198156.3:c.362G>A