Allele Registry

Canonical Allele Identifier: PA2830430568

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV000428620

ClinVar Variation:

376048

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Leu117Gln	CA16602515 NM_198156.3:c.350T>A