Allele Registry

Canonical Allele Identifier: PA2830430910

Gene: VHL HGNC NCBI

ClinVar RCV:

RCV001988653

RCV003464363

ClinVar Variation:

1488572

HGVS (amino-acid)	Matching Registered Transcripts
NP_937799.1:p.Pro151Thr	CA351756433 NM_198156.3:c.451C>A