Allele Registry

Canonical Allele Identifier: PA2830430891

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001316784

ClinVar Variation:

1017610

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Glu145Gln	CA351756383 NM_198156.3:c.433G>C